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rs397507893

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397507893(-;-)
Make rs397507893(-;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32354900
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507893
ebirs397507893
HLIrs397507893
Exacrs397507893
Varsomers397507893
Maprs397507893
PheGenIrs397507893
hapmaprs397507893
1000 genomesrs397507893
hgdprs397507893
ensemblrs397507893
gopubmedrs397507893
geneviewrs397507893
scholarrs397507893
googlers397507893
pharmgkbrs397507893
gwascentralrs397507893
openSNPrs397507893
23andMers397507893
23andMe allrs397507893
SNP Nexus

SNPshotrs397507893
SNPdbers397507893
MSV3drs397507893
GWAS Ctlgrs397507893
Max Magnitude0
ClinVar
Risk rs397507893(;)
Alt rs397507893(;)
Reference rs397507893(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.32929037delT
CLNSRC ClinVar
CLNACC RCV000045127.2,