dbsnp - Robuta Search

https://genebe.net/variant/hg38/rs372736227?mode=cancer dbSNP rs372736227: PTPN11:p.Ala16Ala (chr12-112446309-A-G) – ACMG Classification: Likely_benign (-4... See ACMG classification (Likely_benign, -4) for this variant. Access annotations from ClinVar, UniProt, GnomAD, and more — all gathered in one place with GeneBe a g dbsnp acmg classification likely https://genebe.net/variant/hg38/rs2066713 dbSNP rs2066713: SLC6A4:c.-220-1732CT (chr17-30224647-G-A) – ACMG Classification: Benign (-12 pts)... See ACMG classification (Benign, -12) for this variant. Access annotations from ClinVar, UniProt, GnomAD, and more — all gathered in one place with GeneBe g a dbsnp acmg classification benign https://genebe.net/variant/hg38/rs34580776 dbSNP rs34580776: MYBPC3:p.Arg326Gln (chr11-47346320-C-T) – ACMG Classification: Benign (-10 pts) |... See ACMG classification (Benign, -10) for this variant. Access annotations from ClinVar, UniProt, GnomAD, and more — all gathered in one place with GeneBe c t dbsnp acmg classification benign https://bedrock.bio/datasets/dbsnp/tables/clinvar_disease_xrefs/ dbsnp.clinvar_disease_xrefs | bedrock.bio dbsnp clinvar disease bedrock bio https://genebe.net/variant/hg38/rs4942925?mode=germline dbSNP rs4942925: :null (chr13-32807106-T-C) – ACMG Classification: Benign (-12 pts) | GeneBe See ACMG classification (Benign, -12) for this variant. Access annotations from ClinVar, UniProt, GnomAD, and more — all gathered in one place with GeneBe t c dbsnp null acmg classification https://bioinformaticshome.com/tools/descriptions/Database_of_single_nucleotide_polymorphism__dbSNP_.html Database of single nucleotide polymorphism (dbSNP) Description, details, publications, contact, and download information for Database of single nucleotide polymorphism (dbSNP) database single nucleotide polymorphism dbsnp https://genebe.net/variant/hg38/rs6323 dbSNP rs6323: MAOA:p.Arg297Arg (chrX-43731789-G-T) – ACMG Classification: Benign (-9 pts) | GeneBe See ACMG classification (Benign, -9) for this variant. Access annotations from ClinVar, UniProt, GnomAD, and more — all gathered in one place with GeneBe g t dbsnp maoa chrx acmg https://genebe.net/variant/hg38/rs160343 dbSNP rs160343: CREB5:c.464+55613TA (chr7-28626150-T-A) – ACMG Classification: Likely_benign (-2... See ACMG classification (Likely_benign, -2) for this variant. Access annotations from ClinVar, UniProt, GnomAD, and more — all gathered in one place with GeneBe t a dbsnp acmg classification likely