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rs16956936

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs16956936(C;T)
Make rs16956936(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position7730374
GeneDNAH2
is asnp
is mentioned by
dbSNPrs16956936
ebirs16956936
HLIrs16956936
Exacrs16956936
Varsomers16956936
Maprs16956936
PheGenIrs16956936
hapmaprs16956936
1000 genomesrs16956936
hgdprs16956936
ensemblrs16956936
gopubmedrs16956936
geneviewrs16956936
scholarrs16956936
googlers16956936
pharmgkbrs16956936
gwascentralrs16956936
openSNPrs16956936
23andMers16956936
23andMe allrs16956936
SNP Nexus

SNPshotrs16956936
SNPdbers16956936
MSV3drs16956936
GWAS Ctlgrs16956936
GMAF0.08264
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 5E-7
Odds Ratio 1.09 [1.00-1.19]


GET Evidence
rs16956936
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.0703125
summary