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rs397507994

From SNPedia

Merged intors80359721
Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
(-;T) 6 BRCA2 variant considered pathogenic for breast cancer
Make rs397507994(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32371062
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507994
ClinGenrs397507994
ebirs397507994
HLIrs397507994
Exacrs397507994
Varsomers397507994
Maprs397507994
PheGenIrs397507994
hapmaprs397507994
1000 genomesrs397507994
hgdprs397507994
ensemblrs397507994
gopubmedrs397507994
geneviewrs397507994
scholarrs397507994
googlers397507994
pharmgkbrs397507994
gwascentralrs397507994
openSNPrs397507994
23andMers397507994
23andMe allrs397507994
SNP Nexus

SNPshotrs397507994
SNPdbers397507994
MSV3drs397507994
GWAS Ctlgrs397507994
StatusMerged into rs80359721
Max Magnitude6
ClinVar
Risk rs397507994(T;T)
Alt rs397507994(T;T)
Reference Rs397507994(;)
Significance Pathogenic
Disease Hereditary breast and ovarian cancer syndrome Breast-ovarian cancer Hereditary cancer-predisposing syndrome
Variation info
Gene BRCA2
CLNDBN Hereditary breast and ovarian cancer syndrome Breast-ovarian cancer, familial 2 Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000013.10:g.32945199dupT
CLNSRC Breast Cancer Information Core (BRCA2)
CLNACC RCV000045570.3, RCV000077637.4, RCV000165308.2,