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rs780318765

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs780318765(C;T)
Make rs780318765(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome5
Position170019037
GeneDOCK2
is asnp
is mentioned by
dbSNPrs780318765
ebirs780318765
HLIrs780318765
Exacrs780318765
Varsomers780318765
Maprs780318765
PheGenIrs780318765
hapmaprs780318765
1000 genomesrs780318765
hgdprs780318765
ensemblrs780318765
gopubmedrs780318765
geneviewrs780318765
scholarrs780318765
googlers780318765
pharmgkbrs780318765
gwascentralrs780318765
openSNPrs780318765
23andMers780318765
23andMe allrs780318765
SNP Nexus

SNPshotrs780318765
SNPdbers780318765
MSV3drs780318765
GWAS Ctlgrs780318765
Max Magnitude0
ClinVar
Risk rs780318765(T;T)
Alt rs780318765(T;T)
Reference rs780318765(C;C)
Significance Pathogenic
Disease Immunodeficiency 40
Variation info
Gene DOCK2
CLNDBN Immunodeficiency 40
Reversed 0
HGVS NC_000005.9:g.169446041C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000180782.2,