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rs397507952

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AA;AA) 0 common in clinvar
Make rs397507952(-;-)
Make rs397507952(-;AA)
ReferenceGRCh38 38.1/141
Chromosome13
Position32363222
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507952
ebirs397507952
HLIrs397507952
Exacrs397507952
Varsomers397507952
Maprs397507952
PheGenIrs397507952
hapmaprs397507952
1000 genomesrs397507952
hgdprs397507952
ensemblrs397507952
gopubmedrs397507952
geneviewrs397507952
scholarrs397507952
googlers397507952
pharmgkbrs397507952
gwascentralrs397507952
openSNPrs397507952
23andMers397507952
23andMe allrs397507952
SNP Nexus

SNPshotrs397507952
SNPdbers397507952
MSV3drs397507952
GWAS Ctlgrs397507952
Max Magnitude0
ClinVar
Risk rs397507952(;)
Alt rs397507952(;)
Reference rs397507952(AA;AA)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32937359_32937360delAA
CLNSRC ClinVar
CLNACC RCV000045388.2,