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rs606231393

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs606231393(-;-)
Make rs606231393(-;A)
Make rs606231393(A;A)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position43091907
GeneBRCA1
is asnp
is mentioned by
dbSNPrs606231393
ebirs606231393
HLIrs606231393
Exacrs606231393
Varsomers606231393
Maprs606231393
PheGenIrs606231393
hapmaprs606231393
1000 genomesrs606231393
hgdprs606231393
ensemblrs606231393
gopubmedrs606231393
geneviewrs606231393
scholarrs606231393
googlers606231393
pharmgkbrs606231393
gwascentralrs606231393
openSNPrs606231393
23andMers606231393
23andMe allrs606231393
SNP Nexus

SNPshotrs606231393
SNPdbers606231393
MSV3drs606231393
GWAS Ctlgrs606231393
Max Magnitude0
ClinVar
Risk rs606231393(A;A)
Alt rs606231393(A;A)
Reference rs606231393(;)
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.41243924dupT
CLNSRC Breast Cancer Information Core (BRCA1)
CLNACC RCV000048259.2, RCV000112139.1,