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rs10733113

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0
Make rs10733113(A;A)
Make rs10733113(A;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position247459055
is asnp
is mentioned by
dbSNPrs10733113
ebirs10733113
HLIrs10733113
Exacrs10733113
Varsomers10733113
Maprs10733113
PheGenIrs10733113
hapmaprs10733113
1000 genomesrs10733113
hgdprs10733113
ensemblrs10733113
gopubmedrs10733113
geneviewrs10733113
scholarrs10733113
googlers10733113
pharmgkbrs10733113
gwascentralrs10733113
openSNPrs10733113
23andMers10733113
23andMe allrs10733113
SNP Nexus

SNPshotrs10733113
SNPdbers10733113
MSV3drs10733113
GWAS Ctlgrs10733113
GMAF0.1662
Max Magnitude0
? (A;A) (A;G) (G;G) 28
OMIM606416
DescNLR FAMILY, PYRIN DOMAIN-CONTAINING 3; NLRP3
Variant
Relatedalso
OMIM266600
Desc
Variant
Relatedalso


GET Evidence
rs10733113
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.854839
summary



[PMID 23547871] Genetic variants in CARD8 but not in NLRP3 are associated with ankylosing spondylitis


[PMID 23171454] Genetic support for the role of the NLRP3 inflammasome in psoriasis susceptibility.