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rs397507756

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397507756(-;-)
Make rs397507756(-;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position32339400
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507756
ebirs397507756
HLIrs397507756
Exacrs397507756
Varsomers397507756
Maprs397507756
PheGenIrs397507756
hapmaprs397507756
1000 genomesrs397507756
hgdprs397507756
ensemblrs397507756
gopubmedrs397507756
geneviewrs397507756
scholarrs397507756
googlers397507756
pharmgkbrs397507756
gwascentralrs397507756
openSNPrs397507756
23andMers397507756
23andMe allrs397507756
SNP Nexus

SNPshotrs397507756
SNPdbers397507756
MSV3drs397507756
GWAS Ctlgrs397507756
Max Magnitude0
ClinVar
Risk rs397507756(;)
Alt rs397507756(;)
Reference rs397507756(G;G)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32913537delG
CLNSRC ClinVar
CLNACC RCV000044544.2,