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rs397507760

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397507760(-;-)
Make rs397507760(-;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position32339486
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507760
ebirs397507760
HLIrs397507760
Exacrs397507760
Varsomers397507760
Maprs397507760
PheGenIrs397507760
hapmaprs397507760
1000 genomesrs397507760
hgdprs397507760
ensemblrs397507760
gopubmedrs397507760
geneviewrs397507760
scholarrs397507760
googlers397507760
pharmgkbrs397507760
gwascentralrs397507760
openSNPrs397507760
23andMers397507760
23andMe allrs397507760
SNP Nexus

SNPshotrs397507760
SNPdbers397507760
MSV3drs397507760
GWAS Ctlgrs397507760
Max Magnitude0
ClinVar
Risk rs397507760(;)
Alt rs397507760(;)
Reference rs397507760(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.32913623delG
CLNSRC ClinVar
CLNACC RCV000044565.2,