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rs397507762

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397507762(A;A)
Make rs397507762(A;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position32326283
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507762
ebirs397507762
HLIrs397507762
Exacrs397507762
Varsomers397507762
Maprs397507762
PheGenIrs397507762
hapmaprs397507762
1000 genomesrs397507762
hgdprs397507762
ensemblrs397507762
gopubmedrs397507762
geneviewrs397507762
scholarrs397507762
googlers397507762
pharmgkbrs397507762
gwascentralrs397507762
openSNPrs397507762
23andMers397507762
23andMe allrs397507762
SNP Nexus

SNPshotrs397507762
SNPdbers397507762
MSV3drs397507762
GWAS Ctlgrs397507762
Max Magnitude0
ClinVar
Risk rs397507762(A,C;A,C)
Alt rs397507762(A,C;A,C)
Reference rs397507762(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.32900420G>A; NC_000013.10:g.32900420G>C
CLNSRC ClinVar
CLNACC RCV000044574.2, RCV000044575.2,