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rs397507907

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(CA;CA) 0 common in clinvar
Make rs397507907(-;-)
Make rs397507907(-;CA)
ReferenceGRCh38 38.1/141
Chromosome13
Position32355104
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507907
ebirs397507907
HLIrs397507907
Exacrs397507907
Varsomers397507907
Maprs397507907
PheGenIrs397507907
hapmaprs397507907
1000 genomesrs397507907
hgdprs397507907
ensemblrs397507907
gopubmedrs397507907
geneviewrs397507907
scholarrs397507907
googlers397507907
pharmgkbrs397507907
gwascentralrs397507907
openSNPrs397507907
23andMers397507907
23andMe allrs397507907
SNP Nexus

SNPshotrs397507907
SNPdbers397507907
MSV3drs397507907
GWAS Ctlgrs397507907
Max Magnitude0
ClinVar
Risk rs397507907(;)
Alt rs397507907(;)
Reference rs397507907(CA;CA)
Significance Pathogenic
Disease Hereditary breast and ovarian cancer syndrome Breast-ovarian cancer Hereditary cancer-predisposing syndrome
Variation info
Gene BRCA2
CLNDBN Hereditary breast and ovarian cancer syndrome Breast-ovarian cancer, familial 2 Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000013.10:g.32929241_32929242delCA
CLNSRC ClinVar
CLNACC RCV000045175.5, RCV000083133.2, RCV000166921.1,