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rs397507323

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(GAAA;GAAA) 0 common in clinvar
Make rs397507323(-;-)
Make rs397507323(-;GAAA)
ReferenceGRCh38 38.1/141
Chromosome13
Position32338482
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507323
ebirs397507323
HLIrs397507323
Exacrs397507323
Varsomers397507323
Maprs397507323
PheGenIrs397507323
hapmaprs397507323
1000 genomesrs397507323
hgdprs397507323
ensemblrs397507323
gopubmedrs397507323
geneviewrs397507323
scholarrs397507323
googlers397507323
pharmgkbrs397507323
gwascentralrs397507323
openSNPrs397507323
23andMers397507323
23andMe allrs397507323
SNP Nexus

SNPshotrs397507323
SNPdbers397507323
MSV3drs397507323
GWAS Ctlgrs397507323
Max Magnitude0
ClinVar
Risk rs397507323(;)
Alt rs397507323(;)
Reference rs397507323(GAAA;GAAA)
Significance Pathogenic
Disease Breast-ovarian cancer Hereditary breast and ovarian cancer syndrome
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2 Hereditary breast and ovarian cancer syndrome
Reversed 0
HGVS NC_000013.10:g.32912619_32912622delGAAA
CLNSRC ClinVar
CLNACC RCV000031461.4, RCV000204198.1,