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rs1208285

From SNPedia

Orientationplus
Stabilizedplus
Make rs1208285(C;C)
Make rs1208285(C;T)
Make rs1208285(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position133837662
GeneLINC01312, TARID
is asnp
is mentioned by
dbSNPrs1208285
dbSNP (old)rs1208285
ClinGenrs1208285
ebirs1208285
HLIrs1208285
Exacrs1208285
Gnomadrs1208285
Varsomers1208285
Maprs1208285
PheGenIrs1208285
Biobankrs1208285
1000 genomesrs1208285
hgdprs1208285
ensemblrs1208285
gopubmedrs1208285
geneviewrs1208285
scholarrs1208285
googlers1208285
pharmgkbrs1208285
gwascentralrs1208285
openSNPrs1208285
23andMers1208285
23andMe allrs1208285
SNPshotrs1208285
SNPdbers1208285
MSV3drs1208285
GWAS Ctlgrs1208285
GMAF0.2842
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 22306654OA-icon.png]
Trait
Title Common variants near MBNL1 and NKX2-5 are associated with infantile hypertrophic pyloric stenosis.
Risk Allele C
P-val 6E-7
Odds Ratio 1.2500 None