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rs273585623

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs273585623(A;A)
Make rs273585623(A;C)
ReferenceGRCh38 38.1/142
Chromosome16
Position88433649
GeneZNF469
is asnp
is mentioned by
dbSNPrs273585623
ebirs273585623
HLIrs273585623
Exacrs273585623
Varsomers273585623
Maprs273585623
PheGenIrs273585623
hapmaprs273585623
1000 genomesrs273585623
hgdprs273585623
ensemblrs273585623
gopubmedrs273585623
geneviewrs273585623
scholarrs273585623
googlers273585623
pharmgkbrs273585623
gwascentralrs273585623
openSNPrs273585623
23andMers273585623
23andMe allrs273585623
SNP Nexus

SNPshotrs273585623
SNPdbers273585623
MSV3drs273585623
GWAS Ctlgrs273585623
Max Magnitude0
ClinVar
Risk rs273585623(A;A)
Alt rs273585623(A;A)
Reference rs273585623(C;C)
Significance Pathogenic
Disease Keratoconus 1
Variation info
Gene ZNF469
CLNDBN Keratoconus 1
Reversed 0
HGVS NC_000016.9:g.88500057C>A
CLNSRC ClinVar
CLNACC RCV000114784.1,