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rs113994175

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs113994175(A;T)
Make rs113994175(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position97738085
GeneZAP70
is asnp
is mentioned by
dbSNPrs113994175
ebirs113994175
HLIrs113994175
Exacrs113994175
Varsomers113994175
Maprs113994175
PheGenIrs113994175
hapmaprs113994175
1000 genomesrs113994175
hgdprs113994175
ensemblrs113994175
gopubmedrs113994175
geneviewrs113994175
scholarrs113994175
googlers113994175
pharmgkbrs113994175
gwascentralrs113994175
openSNPrs113994175
23andMers113994175
23andMe allrs113994175
SNP Nexus

SNPshotrs113994175
SNPdbers113994175
MSV3drs113994175
GWAS Ctlgrs113994175
Max Magnitude0
ClinVar
Risk rs113994175(T;T)
Alt rs113994175(T;T)
Reference rs113994175(A;A)
Significance Pathogenic
Disease Cd8 deficiency
Variation info
Gene ZAP70
CLNDBN Cd8 deficiency, familial
Reversed 0
HGVS NC_000002.11:g.98354548A>T
CLNSRC ClinVar GeneReviews
CLNACC RCV000032161.1,