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rs4954218

From SNPedia

Orientationplus
Stabilizedplus
Make rs4954218(G;G)
Make rs4954218(G;T)
Make rs4954218(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position135045855
is asnp
is mentioned by
dbSNPrs4954218
ebirs4954218
HLIrs4954218
Exacrs4954218
Varsomers4954218
Maprs4954218
PheGenIrs4954218
hapmaprs4954218
1000 genomesrs4954218
hgdprs4954218
ensemblrs4954218
gopubmedrs4954218
geneviewrs4954218
scholarrs4954218
googlers4954218
pharmgkbrs4954218
gwascentralrs4954218
openSNPrs4954218
23andMers4954218
23andMe allrs4954218
SNP Nexus

SNPshotrs4954218
SNPdbers4954218
MSV3drs4954218
GWAS Ctlgrs4954218
GMAF0.0978
Max Magnitude
? (G;G) (G;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 1E-9
Odds Ratio 1.6100 [NR]


[PMID 23833071OA-icon.png] Replication and meta-analysis of candidate loci identified variation at RAB3GAP1 associated with keratoconus


[PMID 25675348] Evaluating the Association between Keratoconus and Reported Genetic Loci in a Han Chinese Population