Have questions? Visit https://www.reddit.com/r/SNPedia

rs762909359

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs762909359(C;T)
Make rs762909359(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome5
Position170047513
GeneDOCK2
is asnp
is mentioned by
dbSNPrs762909359
ClinGenrs762909359
ebirs762909359
HLIrs762909359
Exacrs762909359
Varsomers762909359
Maprs762909359
PheGenIrs762909359
hapmaprs762909359
1000 genomesrs762909359
hgdprs762909359
ensemblrs762909359
gopubmedrs762909359
geneviewrs762909359
scholarrs762909359
googlers762909359
pharmgkbrs762909359
gwascentralrs762909359
openSNPrs762909359
23andMers762909359
23andMe allrs762909359
SNP Nexus

SNPshotrs762909359
SNPdbers762909359
MSV3drs762909359
GWAS Ctlgrs762909359
Max Magnitude0
ClinVar
Risk rs762909359(T;T)
Alt rs762909359(T;T)
Reference Rs762909359(C;C)
Significance Pathogenic
Disease Immunodeficiency 40
Variation info
Gene DOCK2
CLNDBN Immunodeficiency 40
Reversed 0
HGVS NC_000005.9:g.169474517C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000180781.2,