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rs273585631

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs273585631(A;A)
Make rs273585631(A;G)
ReferenceGRCh38 38.1/142
Chromosome16
Position88427569
GeneZNF469
is asnp
is mentioned by
dbSNPrs273585631
ebirs273585631
HLIrs273585631
Exacrs273585631
Varsomers273585631
Maprs273585631
PheGenIrs273585631
hapmaprs273585631
1000 genomesrs273585631
hgdprs273585631
ensemblrs273585631
gopubmedrs273585631
geneviewrs273585631
scholarrs273585631
googlers273585631
pharmgkbrs273585631
gwascentralrs273585631
openSNPrs273585631
23andMers273585631
23andMe allrs273585631
SNP Nexus

SNPshotrs273585631
SNPdbers273585631
MSV3drs273585631
GWAS Ctlgrs273585631
Max Magnitude0
ClinVar
Risk rs273585631(A;A)
Alt rs273585631(A;A)
Reference rs273585631(G;G)
Significance Probable-Pathogenic
Disease Keratoconus 1
Variation info
Gene ZNF469
CLNDBN Keratoconus 1
Reversed 0
HGVS NC_000016.9:g.88493977G>A
CLNSRC ClinVar
CLNACC RCV000114792.1,