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rs3771150

From SNPedia

Orientationminus
Stabilizedminus
Make rs3771150(C;C)
Make rs3771150(C;T)
Make rs3771150(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position102444391
GeneIL18RAP
is asnp
is mentioned by
dbSNPrs3771150
ebirs3771150
HLIrs3771150
Exacrs3771150
Varsomers3771150
Maprs3771150
PheGenIrs3771150
hapmaprs3771150
1000 genomesrs3771150
hgdprs3771150
ensemblrs3771150
gopubmedrs3771150
geneviewrs3771150
scholarrs3771150
googlers3771150
pharmgkbrs3771150
gwascentralrs3771150
openSNPrs3771150
23andMers3771150
23andMe allrs3771150
SNP Nexus

SNPshotrs3771150
SNPdbers3771150
MSV3drs3771150
GWAS Ctlgrs3771150
GMAF0.2452
Max Magnitude
? (C;C) (C;T) (T;T) 28

This SNP was associated with amyotrophic lateral sclerosis (ALS) based on a study of 1,152 patients.[PMID 17671248]


[PMID 22289858OA-icon.png] IL-18R1 and IL-18RAP SNPs may be associated with bronchopulmonary dysplasia in African-American infants