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rs62625298

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs62625298(A;A)
Make rs62625298(A;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position43094838
GeneBRCA1
is asnp
is mentioned by
dbSNPrs62625298
ebirs62625298
HLIrs62625298
Exacrs62625298
Varsomers62625298
Maprs62625298
PheGenIrs62625298
hapmaprs62625298
1000 genomesrs62625298
hgdprs62625298
ensemblrs62625298
gopubmedrs62625298
geneviewrs62625298
scholarrs62625298
googlers62625298
pharmgkbrs62625298
gwascentralrs62625298
openSNPrs62625298
23andMers62625298
23andMe allrs62625298
SNP Nexus

SNPshotrs62625298
SNPdbers62625298
MSV3drs62625298
GWAS Ctlgrs62625298
Max Magnitude0
ClinVar
Risk rs62625298(A,T;A,T)
Alt rs62625298(A,T;A,T)
Reference rs62625298(G;G)
Significance Probable-non-pathogenic
Disease Familial cancer of breast Hereditary breast and ovarian cancer syndrome Hereditary cancer-predisposing syndrome Breast-ovarian cancer not specified
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast Hereditary breast and ovarian cancer syndrome Hereditary cancer-predisposing syndrome Breast-ovarian cancer, familial 1 not specified
Reversed 1
HGVS NC_000017.10:g.41246855C>A; NC_000017.10:g.41246855C>T
CLNSRC ClinVar Ambry Genetics Invitae
CLNACC RCV000049100.2, RCV000049099.6, RCV000131383.2, RCV000144222.2, RCV000159943.2,