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rs786205517

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs786205517(C;T)
Make rs786205517(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome19
Position17841711
GeneJAK3
is asnp
is mentioned by
dbSNPrs786205517
ebirs786205517
HLIrs786205517
Exacrs786205517
Varsomers786205517
Maprs786205517
PheGenIrs786205517
hapmaprs786205517
1000 genomesrs786205517
hgdprs786205517
ensemblrs786205517
gopubmedrs786205517
geneviewrs786205517
scholarrs786205517
googlers786205517
pharmgkbrs786205517
gwascentralrs786205517
openSNPrs786205517
23andMers786205517
23andMe allrs786205517
SNP Nexus

SNPshotrs786205517
SNPdbers786205517
MSV3drs786205517
GWAS Ctlgrs786205517
Max Magnitude0
ClinVar
Risk rs786205517(T;T)
Alt rs786205517(T;T)
Reference rs786205517(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene JAK3
CLNDBN not provided
Reversed 1
HGVS NC_000019.9:g.17952520G>A
CLNSRC
CLNACC RCV000171280.1,