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rs397507628

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397507628(A;T)
Make rs397507628(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32319253
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507628
ebirs397507628
HLIrs397507628
Exacrs397507628
Varsomers397507628
Maprs397507628
PheGenIrs397507628
hapmaprs397507628
1000 genomesrs397507628
hgdprs397507628
ensemblrs397507628
gopubmedrs397507628
geneviewrs397507628
scholarrs397507628
googlers397507628
pharmgkbrs397507628
gwascentralrs397507628
openSNPrs397507628
23andMers397507628
23andMe allrs397507628
SNP Nexus

SNPshotrs397507628
SNPdbers397507628
MSV3drs397507628
GWAS Ctlgrs397507628
Max Magnitude0
ClinVar
Risk rs397507628(T;T)
Alt rs397507628(T;T)
Reference rs397507628(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.32893390A>T
CLNSRC ClinVar
CLNACC RCV000043997.2,