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rs10509540

From SNPedia

Orientationplus
Stabilizedplus
Make rs10509540(C;C)
Make rs10509540(C;T)
Make rs10509540(T;T)
ReferenceGRCh38 38.1/142
Chromosome10
Position88263276
GeneLOC101929727, RNLS
is asnp
is mentioned by
dbSNPrs10509540
dbSNP (classic)rs10509540
ClinGenrs10509540
ebirs10509540
HLIrs10509540
Exacrs10509540
Gnomadrs10509540
Varsomers10509540
LitVarrs10509540
Maprs10509540
PheGenIrs10509540
Biobankrs10509540
1000 genomesrs10509540
hgdprs10509540
ensemblrs10509540
geneviewrs10509540
scholarrs10509540
googlers10509540
pharmgkbrs10509540
gwascentralrs10509540
openSNPrs10509540
23andMers10509540
SNPshotrs10509540
SNPdbers10509540
MSV3drs10509540
GWAS Ctlgrs10509540
GMAF0.236
Max Magnitude0
? (C;C) (C;T) (T;T) 28


GWAS snp
PMID [PMID 19430480OA-icon.png]
Trait Type 1 diabetes
Title Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes
Risk Allele
P-val 1E-28
Odds Ratio 1.33 [1.25-1.43]
OMIM222100
Desc
Variant
Relatedalso
OMIM613006
Desc
Variant
Relatedalso



[PMID 22891215OA-icon.png] Evidence of gene-gene interaction and age-at-diagnosis effects in type 1 diabetes.