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rs397507840

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397507840(A;G)
Make rs397507840(G;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position32326616
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507840
ebirs397507840
HLIrs397507840
Exacrs397507840
Varsomers397507840
Maprs397507840
PheGenIrs397507840
hapmaprs397507840
1000 genomesrs397507840
hgdprs397507840
ensemblrs397507840
gopubmedrs397507840
geneviewrs397507840
scholarrs397507840
googlers397507840
pharmgkbrs397507840
gwascentralrs397507840
openSNPrs397507840
23andMers397507840
23andMe allrs397507840
SNP Nexus

SNPshotrs397507840
SNPdbers397507840
MSV3drs397507840
GWAS Ctlgrs397507840
Max Magnitude0
ClinVar
Risk rs397507840(G;G)
Alt rs397507840(G;G)
Reference rs397507840(A;A)
Significance Untested
Disease Hereditary breast and ovarian cancer syndrome
Variation info
Gene BRCA2
CLNDBN Hereditary breast and ovarian cancer syndrome
Reversed 0
HGVS NC_000013.10:g.32900753A>G
CLNSRC ClinVar
CLNACC RCV000044898.3,