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rs397508004

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397508004(-;-)
Make rs397508004(-;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32376767
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397508004
ebirs397508004
HLIrs397508004
Exacrs397508004
Varsomers397508004
Maprs397508004
PheGenIrs397508004
hapmaprs397508004
1000 genomesrs397508004
hgdprs397508004
ensemblrs397508004
gopubmedrs397508004
geneviewrs397508004
scholarrs397508004
googlers397508004
pharmgkbrs397508004
gwascentralrs397508004
openSNPrs397508004
23andMers397508004
23andMe allrs397508004
SNP Nexus

SNPshotrs397508004
SNPdbers397508004
MSV3drs397508004
GWAS Ctlgrs397508004
Max Magnitude0
ClinVar
Risk rs397508004(;)
Alt rs397508004(;)
Reference rs397508004(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.32950904delT
CLNSRC ClinVar
CLNACC RCV000045609.2,