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rs397507781

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397507781(-;-)
Make rs397507781(-;T)
Make rs397507781(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32339710
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507781
ebirs397507781
HLIrs397507781
Exacrs397507781
Varsomers397507781
Maprs397507781
PheGenIrs397507781
hapmaprs397507781
1000 genomesrs397507781
hgdprs397507781
ensemblrs397507781
gopubmedrs397507781
geneviewrs397507781
scholarrs397507781
googlers397507781
pharmgkbrs397507781
gwascentralrs397507781
openSNPrs397507781
23andMers397507781
23andMe allrs397507781
SNP Nexus

SNPshotrs397507781
SNPdbers397507781
MSV3drs397507781
GWAS Ctlgrs397507781
Max Magnitude0
ClinVar
Risk rs397507781(T;T)
Alt rs397507781(T;T)
Reference rs397507781(;)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32913847dupT
CLNSRC ClinVar
CLNACC RCV000044644.2,