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rs195656

From SNPedia

Orientationplus
Stabilizedplus
Make rs195656(A;A)
Make rs195656(A;G)
Make rs195656(G;G)
ReferenceGRCh38 38.1/142
Chromosome16
Position71013581
GeneHYDIN
is asnp
is mentioned by
dbSNPrs195656
ebirs195656
HLIrs195656
Exacrs195656
Varsomers195656
Maprs195656
PheGenIrs195656
hapmaprs195656
1000 genomesrs195656
hgdprs195656
ensemblrs195656
gopubmedrs195656
geneviewrs195656
scholarrs195656
googlers195656
pharmgkbrs195656
gwascentralrs195656
openSNPrs195656
23andMers195656
23andMe allrs195656
SNP Nexus

SNPshotrs195656
SNPdbers195656
MSV3drs195656
GWAS Ctlgrs195656
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 23936387OA-icon.png]
Trait Celiac disease
Title A possible mechanism behind autoimmune disorders discovered by genome-wide linkage and association analysis in celiac disease.
Risk Allele A
P-val 7E-6
Odds Ratio NR NR