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rs606231394

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs606231394(-;-)
Make rs606231394(-;G)
Make rs606231394(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position43051108
GeneBRCA1
is asnp
is mentioned by
dbSNPrs606231394
ebirs606231394
HLIrs606231394
Exacrs606231394
Varsomers606231394
Maprs606231394
PheGenIrs606231394
hapmaprs606231394
1000 genomesrs606231394
hgdprs606231394
ensemblrs606231394
gopubmedrs606231394
geneviewrs606231394
scholarrs606231394
googlers606231394
pharmgkbrs606231394
gwascentralrs606231394
openSNPrs606231394
23andMers606231394
23andMe allrs606231394
SNP Nexus

SNPshotrs606231394
SNPdbers606231394
MSV3drs606231394
GWAS Ctlgrs606231394
Max Magnitude0
ClinVar
Risk rs606231394(G;G)
Alt rs606231394(G;G)
Reference rs606231394(;)
Significance Pathogenic
Disease Familial cancer of breast Breast-ovarian cancer
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast Breast-ovarian cancer, familial 1
Reversed 1
HGVS NC_000017.10:g.41203123dupC
CLNSRC Breast Cancer Information Core (BRCA1)
CLNACC RCV000048912.2, RCV000112602.1,