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rs17006292

From SNPedia

Orientationplus
Stabilizedplus
Make rs17006292(A;A)
Make rs17006292(A;C)
Make rs17006292(C;C)
ReferenceGRCh38 38.1/141
Chromosome2
Position121261187
GeneTFCP2L1
is asnp
is mentioned by
dbSNPrs17006292
ebirs17006292
HLIrs17006292
Exacrs17006292
Varsomers17006292
Maprs17006292
PheGenIrs17006292
hapmaprs17006292
1000 genomesrs17006292
hgdprs17006292
ensemblrs17006292
gopubmedrs17006292
geneviewrs17006292
scholarrs17006292
googlers17006292
pharmgkbrs17006292
gwascentralrs17006292
openSNPrs17006292
23andMers17006292
23andMe allrs17006292
SNP Nexus

SNPshotrs17006292
SNPdbers17006292
MSV3drs17006292
GWAS Ctlgrs17006292
GMAF0.03994
Max Magnitude
? (A;A) (A;C) (C;C) 28
GWAS snp
PMID [PMID 23001997]
Trait Behcet's disease
Title Identification of a susceptibility locus in STAT4 for Behçet's disease in Han Chinese in a genome-wide association study.
Risk Allele
P-val 5E-9
Odds Ratio 4.17 [2.50-5.00]