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rs397507654

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397507654(-;-)
Make rs397507654(-;A)
Make rs397507654(A;A)
ReferenceGRCh38 38.1/141
Chromosome13
Position32319315
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507654
ebirs397507654
HLIrs397507654
Exacrs397507654
Varsomers397507654
Maprs397507654
PheGenIrs397507654
hapmaprs397507654
1000 genomesrs397507654
hgdprs397507654
ensemblrs397507654
gopubmedrs397507654
geneviewrs397507654
scholarrs397507654
googlers397507654
pharmgkbrs397507654
gwascentralrs397507654
openSNPrs397507654
23andMers397507654
23andMe allrs397507654
SNP Nexus

SNPshotrs397507654
SNPdbers397507654
MSV3drs397507654
GWAS Ctlgrs397507654
Max Magnitude0
ClinVar
Risk rs397507654(A;A)
Alt rs397507654(A;A)
Reference rs397507654(;)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32893452dupA
CLNSRC ClinVar
CLNACC RCV000044111.2,