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rs397507915

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(TT;TT) 0 common in clinvar
Make rs397507915(-;-)
Make rs397507915(-;TT)
ReferenceGRCh38 38.1/141
Chromosome13
Position32355261
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507915
ebirs397507915
HLIrs397507915
Exacrs397507915
Varsomers397507915
Maprs397507915
PheGenIrs397507915
hapmaprs397507915
1000 genomesrs397507915
hgdprs397507915
ensemblrs397507915
gopubmedrs397507915
geneviewrs397507915
scholarrs397507915
googlers397507915
pharmgkbrs397507915
gwascentralrs397507915
openSNPrs397507915
23andMers397507915
23andMe allrs397507915
SNP Nexus

SNPshotrs397507915
SNPdbers397507915
MSV3drs397507915
GWAS Ctlgrs397507915
Max Magnitude0
ClinVar
Risk rs397507915(;)
Alt rs397507915(;)
Reference rs397507915(TT;TT)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32929398_32929399delTT
CLNSRC ClinVar
CLNACC RCV000045199.2,