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rs397508968

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
(A;T) 6 BRCA1 variant considered pathogenic for breast cancer
Make rs397508968(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position43093097
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397508968
ClinGenrs397508968
ebirs397508968
HLIrs397508968
Exacrs397508968
Varsomers397508968
Maprs397508968
PheGenIrs397508968
hapmaprs397508968
1000 genomesrs397508968
hgdprs397508968
ensemblrs397508968
gopubmedrs397508968
geneviewrs397508968
scholarrs397508968
googlers397508968
pharmgkbrs397508968
gwascentralrs397508968
openSNPrs397508968
23andMers397508968
23andMe allrs397508968
SNP Nexus

SNPshotrs397508968
SNPdbers397508968
MSV3drs397508968
GWAS Ctlgrs397508968
Max Magnitude6
ClinVar
Risk rs397508968(T;T)
Alt rs397508968(T;T)
Reference Rs397508968(A;A)
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.41245114T>A
CLNSRC ClinVar
CLNACC RCV000047839.2, RCV000256965.2,