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rs397507321

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;G) 6 BRCA2 variant considered pathogenic for breast cancer
(G;G) 0 common in clinvar


Make rs397507321(-;-)
ReferenceGRCh38 38.1/141
Chromosome13
Position32338368
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507321
dbSNP (old)rs397507321
ClinGenrs397507321
ebirs397507321
HLIrs397507321
Exacrs397507321
Gnomadrs397507321
Varsomers397507321
Maprs397507321
PheGenIrs397507321
Biobankrs397507321
1000 genomesrs397507321
hgdprs397507321
ensemblrs397507321
gopubmedrs397507321
geneviewrs397507321
scholarrs397507321
googlers397507321
pharmgkbrs397507321
gwascentralrs397507321
openSNPrs397507321
23andMers397507321
23andMe allrs397507321
SNP Nexus

SNPshotrs397507321
SNPdbers397507321
MSV3drs397507321
GWAS Ctlgrs397507321
Max Magnitude6
ClinVar
Risk rs397507321(-;-)
Alt rs397507321(-;-)
Reference Rs397507321(G;G)
Significance Pathogenic
Disease Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32912505delG
CLNSRC ClinVar
CLNACC RCV000031454.4,