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rs397507754

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397507754(-;-)
Make rs397507754(-;T)
Make rs397507754(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32339354
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507754
ebirs397507754
HLIrs397507754
Exacrs397507754
Varsomers397507754
Maprs397507754
PheGenIrs397507754
hapmaprs397507754
1000 genomesrs397507754
hgdprs397507754
ensemblrs397507754
gopubmedrs397507754
geneviewrs397507754
scholarrs397507754
googlers397507754
pharmgkbrs397507754
gwascentralrs397507754
openSNPrs397507754
23andMers397507754
23andMe allrs397507754
SNP Nexus

SNPshotrs397507754
SNPdbers397507754
MSV3drs397507754
GWAS Ctlgrs397507754
Max Magnitude0
ClinVar
Risk rs397507754(T;T)
Alt rs397507754(T;T)
Reference rs397507754(;)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32913491dupT
CLNSRC ClinVar
CLNACC RCV000044536.2,