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rs10786436

From SNPedia

Orientationplus
Stabilizedplus
Make rs10786436(C;C)
Make rs10786436(C;T)
Make rs10786436(T;T)
ReferenceGRCh38 38.1/142
Chromosome10
Position98540425
GeneHPSE2
is asnp
is mentioned by
dbSNPrs10786436
dbSNP (classic)rs10786436
ClinGenrs10786436
ebirs10786436
HLIrs10786436
Exacrs10786436
Gnomadrs10786436
Varsomers10786436
LitVarrs10786436
Maprs10786436
PheGenIrs10786436
Biobankrs10786436
1000 genomesrs10786436
hgdprs10786436
ensemblrs10786436
geneviewrs10786436
scholarrs10786436
googlers10786436
pharmgkbrs10786436
gwascentralrs10786436
openSNPrs10786436
23andMers10786436
SNPshotrs10786436
SNPdbers10786436
MSV3drs10786436
GWAS Ctlgrs10786436
GMAF0.4371
Max Magnitude0
? (C;C) (C;T) (T;T) 28


GWAS snp
PMID [PMID 21980299OA-icon.png]
Trait
Title A genome-wide meta-analysis of six type 1 diabetes cohorts identifies multiple associated loci.
Risk Allele T
P-val 8E-7
Odds Ratio 1.1000 [NR]