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rs397507613

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397507613(-;-)
Make rs397507613(-;TT)
Make rs397507613(TT;TT)
ReferenceGRCh38 38.1/141
Chromosome13
Position32333377
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507613
ebirs397507613
HLIrs397507613
Exacrs397507613
Varsomers397507613
Maprs397507613
PheGenIrs397507613
hapmaprs397507613
1000 genomesrs397507613
hgdprs397507613
ensemblrs397507613
gopubmedrs397507613
geneviewrs397507613
scholarrs397507613
googlers397507613
pharmgkbrs397507613
gwascentralrs397507613
openSNPrs397507613
23andMers397507613
23andMe allrs397507613
SNP Nexus

SNPshotrs397507613
SNPdbers397507613
MSV3drs397507613
GWAS Ctlgrs397507613
Max Magnitude0
ClinVar
Risk rs397507613(TT;TT)
Alt rs397507613(TT;TT)
Reference rs397507613(;)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32907514_32907515insTT
CLNSRC ClinVar
CLNACC RCV000043919.2,