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rs4871297

From SNPedia

Orientationplus
Stabilizedplus
Make rs4871297(A;A)
Make rs4871297(A;G)
Make rs4871297(G;G)
ReferenceGRCh38 38.1/141
Chromosome8
Position122693916
GeneLINC01151
is asnp
is mentioned by
dbSNPrs4871297
dbSNP (classic)rs4871297
ClinGenrs4871297
ebirs4871297
HLIrs4871297
Exacrs4871297
Gnomadrs4871297
Varsomers4871297
LitVarrs4871297
Maprs4871297
PheGenIrs4871297
Biobankrs4871297
1000 genomesrs4871297
hgdprs4871297
ensemblrs4871297
geneviewrs4871297
scholarrs4871297
googlers4871297
pharmgkbrs4871297
gwascentralrs4871297
openSNPrs4871297
23andMers4871297
SNPshotrs4871297
SNPdbers4871297
MSV3drs4871297
GWAS Ctlgrs4871297
GMAF0.4504
Max Magnitude0
? (A;A) (A;G) (G;G) 28


GWAS snp
PMID [PMID 23028342OA-icon.png]
Trait Type 1 diabetes nephropathy
Title New susceptibility loci associated with kidney disease in type 1 diabetes.
Risk Allele A
P-val 2E-6
Odds Ratio 1.23 [1.14-1.35]