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rs786202631

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786202631(A;A)
Make rs786202631(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position43074483
GeneBRCA1
is asnp
is mentioned by
dbSNPrs786202631
ebirs786202631
HLIrs786202631
Exacrs786202631
Varsomers786202631
Maprs786202631
PheGenIrs786202631
hapmaprs786202631
1000 genomesrs786202631
hgdprs786202631
ensemblrs786202631
gopubmedrs786202631
geneviewrs786202631
scholarrs786202631
googlers786202631
pharmgkbrs786202631
gwascentralrs786202631
openSNPrs786202631
23andMers786202631
23andMe allrs786202631
SNP Nexus

SNPshotrs786202631
SNPdbers786202631
MSV3drs786202631
GWAS Ctlgrs786202631
Max Magnitude0
ClinVar
Risk rs786202631(A;A)
Alt rs786202631(A;A)
Reference rs786202631(G;G)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene BRCA1
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000017.10:g.41226500C>T
CLNSRC
CLNACC RCV000165536.1,