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rs397507856

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397507856(-;-)
Make rs397507856(-;A)
ReferenceGRCh38 38.1/141
Chromosome13
Position32340800
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507856
ebirs397507856
HLIrs397507856
Exacrs397507856
Varsomers397507856
Maprs397507856
PheGenIrs397507856
hapmaprs397507856
1000 genomesrs397507856
hgdprs397507856
ensemblrs397507856
gopubmedrs397507856
geneviewrs397507856
scholarrs397507856
googlers397507856
pharmgkbrs397507856
gwascentralrs397507856
openSNPrs397507856
23andMers397507856
23andMe allrs397507856
SNP Nexus

SNPshotrs397507856
SNPdbers397507856
MSV3drs397507856
GWAS Ctlgrs397507856
Max Magnitude0
ClinVar
Risk rs397507856(;)
Alt rs397507856(;)
Reference rs397507856(A;A)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32914937delA
CLNSRC ClinVar
CLNACC RCV000044954.2,