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rs397507353

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397507353(-;-)
Make rs397507353(-;A)
ReferenceGRCh38 38.1/141
Chromosome13
Position32339853
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507353
ebirs397507353
HLIrs397507353
Exacrs397507353
Varsomers397507353
Maprs397507353
PheGenIrs397507353
hapmaprs397507353
1000 genomesrs397507353
hgdprs397507353
ensemblrs397507353
gopubmedrs397507353
geneviewrs397507353
scholarrs397507353
googlers397507353
pharmgkbrs397507353
gwascentralrs397507353
openSNPrs397507353
23andMers397507353
23andMe allrs397507353
SNP Nexus

SNPshotrs397507353
SNPdbers397507353
MSV3drs397507353
GWAS Ctlgrs397507353
Max Magnitude0
ClinVar
Risk rs397507353(;)
Alt rs397507353(;)
Reference rs397507353(A;A)
Significance Pathogenic
Disease Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32913990delA
CLNSRC ClinVar
CLNACC RCV000031551.3,