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rs273585637

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs273585637(C;T)
Make rs273585637(T;T)
ReferenceGRCh38 38.1/142
Chromosome16
Position88438397
GeneZNF469
is asnp
is mentioned by
dbSNPrs273585637
ebirs273585637
HLIrs273585637
Exacrs273585637
Varsomers273585637
Maprs273585637
PheGenIrs273585637
hapmaprs273585637
1000 genomesrs273585637
hgdprs273585637
ensemblrs273585637
gopubmedrs273585637
geneviewrs273585637
scholarrs273585637
googlers273585637
pharmgkbrs273585637
gwascentralrs273585637
openSNPrs273585637
23andMers273585637
23andMe allrs273585637
SNP Nexus

SNPshotrs273585637
SNPdbers273585637
MSV3drs273585637
GWAS Ctlgrs273585637
Max Magnitude0
ClinVar
Risk rs273585637(T;T)
Alt rs273585637(T;T)
Reference rs273585637(C;C)
Significance Probable-Pathogenic
Disease Keratoconus 1
Variation info
Gene ZNF469
CLNDBN Keratoconus 1
Reversed 0
HGVS NC_000016.9:g.88504805C>T
CLNSRC ClinVar
CLNACC RCV000114773.1,