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rs2233945

From SNPedia

Orientationminus
Stabilizedminus
Make rs2233945(G;G)
Make rs2233945(G;T)
Make rs2233945(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31139584
GenePSORS1C1, PSORS1C2
is asnp
is mentioned by
dbSNPrs2233945
ebirs2233945
HLIrs2233945
Exacrs2233945
Varsomers2233945
Maprs2233945
PheGenIrs2233945
hapmaprs2233945
1000 genomesrs2233945
hgdprs2233945
ensemblrs2233945
gopubmedrs2233945
geneviewrs2233945
scholarrs2233945
googlers2233945
pharmgkbrs2233945
gwascentralrs2233945
openSNPrs2233945
23andMers2233945
23andMe allrs2233945
SNP Nexus

SNPshotrs2233945
SNPdbers2233945
MSV3drs2233945
GWAS Ctlgrs2233945
GMAF0.1221
Max Magnitude
? (G;G) (G;T) (T;T) 28

[PMID 24322967] HCP5 genetic variant (RS3099844) contributes to Nevirapine-induced Stevens Johnsons Syndrome/Toxic Epidermal Necrolysis susceptibility in a population from Mozambique


[PMID 27342690] Polymorphisms in STAT4, IL10, PSORS1C1, PTPN2 and MIR146A genes are differently associated with prognostic factors in Italian patients affected by Rheumatoid Arthritis.