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rs1057518028

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057518028(C;T)
Make rs1057518028(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome9
Position340290
GeneDOCK8
is asnp
is mentioned by
dbSNPrs1057518028
dbSNP (old)rs1057518028
ClinGenrs1057518028
ebirs1057518028
HLIrs1057518028
Exacrs1057518028
Gnomadrs1057518028
Varsomers1057518028
Maprs1057518028
PheGenIrs1057518028
Biobankrs1057518028
1000 genomesrs1057518028
hgdprs1057518028
ensemblrs1057518028
gopubmedrs1057518028
geneviewrs1057518028
scholarrs1057518028
googlers1057518028
pharmgkbrs1057518028
gwascentralrs1057518028
openSNPrs1057518028
23andMers1057518028
23andMe allrs1057518028
SNPshotrs1057518028
SNPdbers1057518028
MSV3drs1057518028
GWAS Ctlgrs1057518028
Max Magnitude0
ClinVar
Risk rs1057518028(T;T)
Alt rs1057518028(T;T)
Reference Rs1057518028(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene DOCK8
CLNDBN not provided
Reversed 0
HGVS NC_000009.11:g.340290C>T
CLNSRC
CLNACC RCV000412782.1,