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rs397507914

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397507914(-;-)
Make rs397507914(-;A)
ReferenceGRCh38 38.1/141
Chromosome13
Position32355232
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507914
ebirs397507914
HLIrs397507914
Exacrs397507914
Varsomers397507914
Maprs397507914
PheGenIrs397507914
hapmaprs397507914
1000 genomesrs397507914
hgdprs397507914
ensemblrs397507914
gopubmedrs397507914
geneviewrs397507914
scholarrs397507914
googlers397507914
pharmgkbrs397507914
gwascentralrs397507914
openSNPrs397507914
23andMers397507914
23andMe allrs397507914
SNP Nexus

SNPshotrs397507914
SNPdbers397507914
MSV3drs397507914
GWAS Ctlgrs397507914
Max Magnitude0
ClinVar
Risk rs397507914(;)
Alt rs397507914(;)
Reference rs397507914(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.32929369delA
CLNSRC ClinVar
CLNACC RCV000045195.2,