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rs779037308

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs779037308(A;A)
Make rs779037308(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome19
Position10351093
GeneTYK2
is asnp
is mentioned by
dbSNPrs779037308
dbSNP (classic)rs779037308
ClinGenrs779037308
ebirs779037308
HLIrs779037308
Exacrs779037308
Gnomadrs779037308
Varsomers779037308
LitVarrs779037308
Maprs779037308
PheGenIrs779037308
Biobankrs779037308
1000 genomesrs779037308
hgdprs779037308
ensemblrs779037308
geneviewrs779037308
scholarrs779037308
googlers779037308
pharmgkbrs779037308
gwascentralrs779037308
openSNPrs779037308
23andMers779037308
23andMe allrs779037308
SNPshotrs779037308
SNPdbers779037308
MSV3drs779037308
GWAS Ctlgrs779037308
Max Magnitude0
ClinVar
Risk rs779037308(A;A) rs779037308(C;C)
Alt rs779037308(A;A) rs779037308(C;C)
Reference Rs779037308(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TYK2
CLNDBN not provided
Reversed 0
HGVS NC_000019.9:g.10461769G>A
CLNSRC
CLNACC RCV000489725.1,