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rs397507215

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397507215(C;T)
Make rs397507215(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position43092179
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397507215
ebirs397507215
HLIrs397507215
Exacrs397507215
Varsomers397507215
Maprs397507215
PheGenIrs397507215
hapmaprs397507215
1000 genomesrs397507215
hgdprs397507215
ensemblrs397507215
gopubmedrs397507215
geneviewrs397507215
scholarrs397507215
googlers397507215
pharmgkbrs397507215
gwascentralrs397507215
openSNPrs397507215
23andMers397507215
23andMe allrs397507215
SNP Nexus

SNPshotrs397507215
SNPdbers397507215
MSV3drs397507215
GWAS Ctlgrs397507215
Max Magnitude0
ClinVar
Risk rs397507215(T;T)
Alt rs397507215(T;T)
Reference rs397507215(C;C)
Significance Pathogenic
Disease Breast-ovarian cancer Hereditary cancer-predisposing syndrome
Variation info
Gene BRCA1
CLNDBN Breast-ovarian cancer, familial 1 Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000017.10:g.41244196G>A
CLNSRC ClinVar
CLNACC RCV000031105.3, RCV000167367.1,