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rs273585624

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs273585624(A;A)
Make rs273585624(A;C)
ReferenceGRCh38 38.1/142
Chromosome16
Position88434279
GeneZNF469
is asnp
is mentioned by
dbSNPrs273585624
ebirs273585624
HLIrs273585624
Exacrs273585624
Varsomers273585624
Maprs273585624
PheGenIrs273585624
hapmaprs273585624
1000 genomesrs273585624
hgdprs273585624
ensemblrs273585624
gopubmedrs273585624
geneviewrs273585624
scholarrs273585624
googlers273585624
pharmgkbrs273585624
gwascentralrs273585624
openSNPrs273585624
23andMers273585624
23andMe allrs273585624
SNP Nexus

SNPshotrs273585624
SNPdbers273585624
MSV3drs273585624
GWAS Ctlgrs273585624
Max Magnitude0
ClinVar
Risk rs273585624(A;A)
Alt rs273585624(A;A)
Reference rs273585624(C;C)
Significance Pathogenic
Disease Keratoconus 1
Variation info
Gene ZNF469
CLNDBN Keratoconus 1
Reversed 0
HGVS NC_000016.9:g.88500687C>A
CLNSRC ClinVar
CLNACC RCV000114785.1,