Have questions? Visit https://www.reddit.com/r/SNPedia

rs8111998

From SNPedia

Orientationplus
Stabilizedplus
Make rs8111998(C;C)
Make rs8111998(C;T)
Make rs8111998(T;T)
ReferenceGRCh38 38.1/141
Chromosome19
Position22558873
is asnp
is mentioned by
dbSNPrs8111998
ClinGenrs8111998
ebirs8111998
HLIrs8111998
Exacrs8111998
Varsomers8111998
Maprs8111998
PheGenIrs8111998
hapmaprs8111998
1000 genomesrs8111998
hgdprs8111998
ensemblrs8111998
gopubmedrs8111998
geneviewrs8111998
scholarrs8111998
googlers8111998
pharmgkbrs8111998
gwascentralrs8111998
openSNPrs8111998
23andMers8111998
23andMe allrs8111998
SNP Nexus

SNPshotrs8111998
SNPdbers8111998
MSV3drs8111998
GWAS Ctlgrs8111998
GMAF0.2218
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 21979947OA-icon.png]
Trait
Title A genome-wide association study identifies a potential novel gene locus for keratoconus, one of the commonest causes for corneal transplantation in developed countries.
Risk Allele
P-val 8E-7
Odds Ratio 1.7100 [NR]