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rs273585625

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs273585625(G;T)
Make rs273585625(T;T)
ReferenceGRCh38 38.1/142
Chromosome16
Position88436466
GeneZNF469
is asnp
is mentioned by
dbSNPrs273585625
ebirs273585625
HLIrs273585625
Exacrs273585625
Varsomers273585625
Maprs273585625
PheGenIrs273585625
hapmaprs273585625
1000 genomesrs273585625
hgdprs273585625
ensemblrs273585625
gopubmedrs273585625
geneviewrs273585625
scholarrs273585625
googlers273585625
pharmgkbrs273585625
gwascentralrs273585625
openSNPrs273585625
23andMers273585625
23andMe allrs273585625
SNP Nexus

SNPshotrs273585625
SNPdbers273585625
MSV3drs273585625
GWAS Ctlgrs273585625
Max Magnitude0
ClinVar
Risk rs273585625(T;T)
Alt rs273585625(T;T)
Reference rs273585625(G;G)
Significance Pathogenic
Disease Keratoconus 1
Variation info
Gene ZNF469
CLNDBN Keratoconus 1
Reversed 0
HGVS NC_000016.9:g.88502874G>T
CLNSRC ClinVar
CLNACC RCV000114788.1,