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rs397514259

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397514259(A;A)
Make rs397514259(A;G)
ReferenceGRCh38 38.1/141
Chromosome14
Position22550664
GeneTRA@
is asnp
is mentioned by
dbSNPrs397514259
ebirs397514259
HLIrs397514259
Exacrs397514259
Varsomers397514259
Maprs397514259
PheGenIrs397514259
hapmaprs397514259
1000 genomesrs397514259
hgdprs397514259
ensemblrs397514259
gopubmedrs397514259
geneviewrs397514259
scholarrs397514259
googlers397514259
pharmgkbrs397514259
gwascentralrs397514259
openSNPrs397514259
23andMers397514259
23andMe allrs397514259
SNP Nexus

SNPshotrs397514259
SNPdbers397514259
MSV3drs397514259
GWAS Ctlgrs397514259
Max Magnitude0
ClinVar
Risk rs397514259(A;A)
Alt rs397514259(A;A)
Reference rs397514259(G;G)
Significance Pathogenic
Disease T-cell receptor alpha/beta deficiency
Variation info
Gene
CLNDBN T-cell receptor alpha/beta deficiency
Reversed 0
HGVS NC_000014.8:g.23019608G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000054556.17,