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rs397507860

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397507860(C;T)
Make rs397507860(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32340845
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507860
ClinGenrs397507860
ebirs397507860
HLIrs397507860
Exacrs397507860
Varsomers397507860
Maprs397507860
PheGenIrs397507860
hapmaprs397507860
1000 genomesrs397507860
hgdprs397507860
ensemblrs397507860
gopubmedrs397507860
geneviewrs397507860
scholarrs397507860
googlers397507860
pharmgkbrs397507860
gwascentralrs397507860
openSNPrs397507860
23andMers397507860
23andMe allrs397507860
SNP Nexus

SNPshotrs397507860
SNPdbers397507860
MSV3drs397507860
GWAS Ctlgrs397507860
Max Magnitude0
ClinVar
Risk rs397507860(T;T)
Alt rs397507860(T;T)
Reference Rs397507860(C;C)
Significance Pathogenic
Disease Hereditary breast and ovarian cancer syndrome Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Hereditary breast and ovarian cancer syndrome Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32914982C>T
CLNSRC ClinVar
CLNACC RCV000044968.4, RCV000241068.2,