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rs397507963

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(CT;CT) 0 common in clinvar
(TC;TC) 0 common in clinvar
Make rs397507963(-;-)
Make rs397507963(-;CT)
ReferenceGRCh38 38.1/141
Chromosome13
Position32363274
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507963
ebirs397507963
HLIrs397507963
Exacrs397507963
Varsomers397507963
Maprs397507963
PheGenIrs397507963
hapmaprs397507963
1000 genomesrs397507963
hgdprs397507963
ensemblrs397507963
gopubmedrs397507963
geneviewrs397507963
scholarrs397507963
googlers397507963
pharmgkbrs397507963
gwascentralrs397507963
openSNPrs397507963
23andMers397507963
23andMe allrs397507963
SNP Nexus

SNPshotrs397507963
SNPdbers397507963
MSV3drs397507963
GWAS Ctlgrs397507963
Max Magnitude0
ClinVar
Risk rs397507963(;)
Alt rs397507963(;)
Reference rs397507963(TC;TC)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32937411_32937412delCT
CLNSRC ClinVar
CLNACC RCV000045415.2,