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rs397507921

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
(A;T) 6 BRCA2 variant considered pathogenic for breast cancer
Make rs397507921(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32356604
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507921
dbSNP (old)rs397507921
ClinGenrs397507921
ebirs397507921
HLIrs397507921
Exacrs397507921
Varsomers397507921
Maprs397507921
PheGenIrs397507921
Biobankrs397507921
1000 genomesrs397507921
hgdprs397507921
ensemblrs397507921
gopubmedrs397507921
geneviewrs397507921
scholarrs397507921
googlers397507921
pharmgkbrs397507921
gwascentralrs397507921
openSNPrs397507921
23andMers397507921
23andMe allrs397507921
SNP Nexus

SNPshotrs397507921
SNPdbers397507921
MSV3drs397507921
GWAS Ctlgrs397507921
Max Magnitude6
ClinVar
Risk rs397507921(G;G) rs397507921(T;T)
Alt rs397507921(G;G) rs397507921(T;T)
Reference Rs397507921(A;A)
Significance Pathogenic
Disease Breast-ovarian cancer Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2 Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32930741A>G; NC_000013.10:g.32930741A>T
CLNSRC ClinVar
CLNACC RCV000077001.2, RCV000045258.2, RCV000257025.2,