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rs606231395

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs606231395(-;-)
Make rs606231395(-;T)
Make rs606231395(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position43049142
GeneBRCA1
is asnp
is mentioned by
dbSNPrs606231395
ebirs606231395
HLIrs606231395
Exacrs606231395
Varsomers606231395
Maprs606231395
PheGenIrs606231395
hapmaprs606231395
1000 genomesrs606231395
hgdprs606231395
ensemblrs606231395
gopubmedrs606231395
geneviewrs606231395
scholarrs606231395
googlers606231395
pharmgkbrs606231395
gwascentralrs606231395
openSNPrs606231395
23andMers606231395
23andMe allrs606231395
SNP Nexus

SNPshotrs606231395
SNPdbers606231395
MSV3drs606231395
GWAS Ctlgrs606231395
Max Magnitude0
ClinVar
Risk rs606231395(T;T)
Alt rs606231395(T;T)
Reference rs606231395(;)
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.41201158dupA
CLNSRC Breast Cancer Information Core (BRCA1)
CLNACC RCV000048969.2, RCV000112631.1,