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rs273585629

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs273585629(A;A)
Make rs273585629(A;G)
ReferenceGRCh38 38.1/142
Chromosome16
Position88438655
GeneZNF469
is asnp
is mentioned by
dbSNPrs273585629
ebirs273585629
HLIrs273585629
Exacrs273585629
Varsomers273585629
Maprs273585629
PheGenIrs273585629
hapmaprs273585629
1000 genomesrs273585629
hgdprs273585629
ensemblrs273585629
gopubmedrs273585629
geneviewrs273585629
scholarrs273585629
googlers273585629
pharmgkbrs273585629
gwascentralrs273585629
openSNPrs273585629
23andMers273585629
23andMe allrs273585629
SNP Nexus

SNPshotrs273585629
SNPdbers273585629
MSV3drs273585629
GWAS Ctlgrs273585629
Max Magnitude0
ClinVar
Risk rs273585629(A;A)
Alt rs273585629(A;A)
Reference rs273585629(G;G)
Significance Pathogenic
Disease Keratoconus 1
Variation info
Gene ZNF469
CLNDBN Keratoconus 1
Reversed 0
HGVS NC_000016.9:g.88505063G>A
CLNSRC ClinVar
CLNACC RCV000114774.1,