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rs3823355

From SNPedia

Orientationplus
Stabilizedplus
Make rs3823355(C;C)
Make rs3823355(C;T)
Make rs3823355(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position29974306
GeneHCG9
is asnp
is mentioned by
dbSNPrs3823355
ebirs3823355
HLIrs3823355
Exacrs3823355
Varsomers3823355
Maprs3823355
PheGenIrs3823355
hapmaprs3823355
1000 genomesrs3823355
hgdprs3823355
ensemblrs3823355
gopubmedrs3823355
geneviewrs3823355
scholarrs3823355
googlers3823355
pharmgkbrs3823355
gwascentralrs3823355
openSNPrs3823355
23andMers3823355
23andMe allrs3823355
SNP Nexus

SNPshotrs3823355
SNPdbers3823355
MSV3drs3823355
GWAS Ctlgrs3823355
GMAF0.2805
Max Magnitude
? (C;C) (C;T) (T;T) 28
Generalized Vitiligo


[PMID 19010793OA-icon.png] Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis.


[PMID 20593013OA-icon.png] A major histocompatibility Class I locus contributes to multiple sclerosis susceptibility independently from HLA-DRB1*15:01.

GWAS snp
PMID [PMID 20410501OA-icon.png]
Trait Vitiligo
Title Variant of TYR and autoimmunity susceptibility loci in generalized vitiligo.
Risk Allele T
P-val 9E-23
Odds Ratio 1.50 [1.39-1.63]