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rs397507218

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(GG;GG) 0 common in clinvar
Make rs397507218(C;C)
Make rs397507218(C;GG)
ReferenceGRCh38 38.1/141
Chromosome17
Position43091759
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397507218
ebirs397507218
HLIrs397507218
Exacrs397507218
Varsomers397507218
Maprs397507218
PheGenIrs397507218
hapmaprs397507218
1000 genomesrs397507218
hgdprs397507218
ensemblrs397507218
gopubmedrs397507218
geneviewrs397507218
scholarrs397507218
googlers397507218
pharmgkbrs397507218
gwascentralrs397507218
openSNPrs397507218
23andMers397507218
23andMe allrs397507218
SNP Nexus

SNPshotrs397507218
SNPdbers397507218
MSV3drs397507218
GWAS Ctlgrs397507218
Max Magnitude0
ClinVar
Risk rs397507218(C;C)
Alt rs397507218(C;C)
Reference rs397507218(GG;GG)
Significance Pathogenic
Disease Breast-ovarian cancer
Variation info
Gene BRCA1
CLNDBN Breast-ovarian cancer, familial 1
Reversed 1
HGVS NC_000017.10:g.41243776_41243777delCCinsG
CLNSRC ClinVar
CLNACC RCV000031128.4,