Have questions? Visit https://www.reddit.com/r/SNPedia

rs397507579

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397507579(G;T)
Make rs397507579(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32332805
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507579
ebirs397507579
HLIrs397507579
Exacrs397507579
Varsomers397507579
Maprs397507579
PheGenIrs397507579
hapmaprs397507579
1000 genomesrs397507579
hgdprs397507579
ensemblrs397507579
gopubmedrs397507579
geneviewrs397507579
scholarrs397507579
googlers397507579
pharmgkbrs397507579
gwascentralrs397507579
openSNPrs397507579
23andMers397507579
23andMe allrs397507579
SNP Nexus

SNPshotrs397507579
SNPdbers397507579
MSV3drs397507579
GWAS Ctlgrs397507579
Max Magnitude0
ClinVar
Risk rs397507579(T;T)
Alt rs397507579(T;T)
Reference rs397507579(G;G)
Significance Pathogenic
Disease Familial cancer of breast Breast-ovarian cancer Hereditary breast and ovarian cancer syndrome
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast Breast-ovarian cancer, familial 2 Hereditary breast and ovarian cancer syndrome
Reversed 0
HGVS NC_000013.10:g.32906942G>T
CLNSRC ClinVar
CLNACC RCV000043782.2, RCV000169567.1, RCV000238757.1,