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rs786205596

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs786205596(A;C)
Make rs786205596(C;C)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position368196
GeneDOCK8
is asnp
is mentioned by
dbSNPrs786205596
ebirs786205596
HLIrs786205596
Exacrs786205596
Varsomers786205596
Maprs786205596
PheGenIrs786205596
hapmaprs786205596
1000 genomesrs786205596
hgdprs786205596
ensemblrs786205596
gopubmedrs786205596
geneviewrs786205596
scholarrs786205596
googlers786205596
pharmgkbrs786205596
gwascentralrs786205596
openSNPrs786205596
23andMers786205596
23andMe allrs786205596
SNP Nexus

SNPshotrs786205596
SNPdbers786205596
MSV3drs786205596
GWAS Ctlgrs786205596
Max Magnitude0
ClinVar
Risk rs786205596(C;C)
Alt rs786205596(C;C)
Reference rs786205596(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene DOCK8
CLNDBN not provided
Reversed 0
HGVS NC_000009.11:g.368196A>C
CLNSRC
CLNACC RCV000171422.1,