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rs35018800

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs35018800(A;A)
Make rs35018800(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome19
Position10354167
GeneTYK2
is asnp
is mentioned by
dbSNPrs35018800
dbSNP (old)rs35018800
ClinGenrs35018800
ebirs35018800
HLIrs35018800
Exacrs35018800
Gnomadrs35018800
Varsomers35018800
Maprs35018800
PheGenIrs35018800
Biobankrs35018800
1000 genomesrs35018800
hgdprs35018800
ensemblrs35018800
gopubmedrs35018800
geneviewrs35018800
scholarrs35018800
googlers35018800
pharmgkbrs35018800
gwascentralrs35018800
openSNPrs35018800
23andMers35018800
23andMe allrs35018800
SNP Nexus

SNPshotrs35018800
SNPdbers35018800
MSV3drs35018800
GWAS Ctlgrs35018800
Max Magnitude0

[PMID 26338038] Influence of TYK2 in systemic sclerosis susceptibility: a new locus in the IL-12 pathway

ClinVar
Risk rs35018800(A;A)
Alt rs35018800(A;A)
Reference Rs35018800(G;G)
Significance Probable-non-pathogenic
Disease not specified
Variation info
Gene TYK2
CLNDBN not specified
Reversed 0
HGVS NC_000019.9:g.10464843G>A
CLNSRC
CLNACC RCV000284384.1,


GET Evidence
TYK2-A928V
aa_change Ala928Val
aa_change_short A928V
impact benign
qualified_impact Low clinical importance, Uncertain benign
overall_frequency 0.00585611
summary Probably benign.