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rs397507778

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397507778(C;G)
Make rs397507778(G;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position32339646
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507778
ebirs397507778
HLIrs397507778
Exacrs397507778
Varsomers397507778
Maprs397507778
PheGenIrs397507778
hapmaprs397507778
1000 genomesrs397507778
hgdprs397507778
ensemblrs397507778
gopubmedrs397507778
geneviewrs397507778
scholarrs397507778
googlers397507778
pharmgkbrs397507778
gwascentralrs397507778
openSNPrs397507778
23andMers397507778
23andMe allrs397507778
SNP Nexus

SNPshotrs397507778
SNPdbers397507778
MSV3drs397507778
GWAS Ctlgrs397507778
Max Magnitude0
ClinVar
Risk rs397507778(G;G)
Alt rs397507778(G;G)
Reference rs397507778(C;C)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32913783C>G
CLNSRC ClinVar
CLNACC RCV000044630.2,