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rs397507418

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397507418(-;-)
Make rs397507418(-;TT)
Make rs397507418(TT;TT)
ReferenceGRCh38 38.1/141
Chromosome13
Position32379856
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507418
ebirs397507418
HLIrs397507418
Exacrs397507418
Varsomers397507418
Maprs397507418
PheGenIrs397507418
hapmaprs397507418
1000 genomesrs397507418
hgdprs397507418
ensemblrs397507418
gopubmedrs397507418
geneviewrs397507418
scholarrs397507418
googlers397507418
pharmgkbrs397507418
gwascentralrs397507418
openSNPrs397507418
23andMers397507418
23andMe allrs397507418
SNP Nexus

SNPshotrs397507418
SNPdbers397507418
MSV3drs397507418
GWAS Ctlgrs397507418
Max Magnitude0
ClinVar
Risk rs397507418(TT;TT)
Alt rs397507418(TT;TT)
Reference rs397507418(;)
Significance Pathogenic
Disease Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32953993_32953994insTT
CLNSRC ClinVar
CLNACC RCV000031789.3,