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rs397507592

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397507592(-;-)
Make rs397507592(-;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32332992
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507592
ebirs397507592
HLIrs397507592
Exacrs397507592
Varsomers397507592
Maprs397507592
PheGenIrs397507592
hapmaprs397507592
1000 genomesrs397507592
hgdprs397507592
ensemblrs397507592
gopubmedrs397507592
geneviewrs397507592
scholarrs397507592
googlers397507592
pharmgkbrs397507592
gwascentralrs397507592
openSNPrs397507592
23andMers397507592
23andMe allrs397507592
SNP Nexus

SNPshotrs397507592
SNPdbers397507592
MSV3drs397507592
GWAS Ctlgrs397507592
Max Magnitude0
ClinVar
Risk rs397507592(;)
Alt rs397507592(;)
Reference rs397507592(T;T)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32907129delT
CLNSRC ClinVar
CLNACC RCV000043821.2,