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rs273585626

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs273585626(C;T)
Make rs273585626(T;T)
ReferenceGRCh38 38.1/142
Chromosome16
Position88436601
GeneZNF469
is asnp
is mentioned by
dbSNPrs273585626
ebirs273585626
HLIrs273585626
Exacrs273585626
Varsomers273585626
Maprs273585626
PheGenIrs273585626
hapmaprs273585626
1000 genomesrs273585626
hgdprs273585626
ensemblrs273585626
gopubmedrs273585626
geneviewrs273585626
scholarrs273585626
googlers273585626
pharmgkbrs273585626
gwascentralrs273585626
openSNPrs273585626
23andMers273585626
23andMe allrs273585626
SNP Nexus

SNPshotrs273585626
SNPdbers273585626
MSV3drs273585626
GWAS Ctlgrs273585626
Max Magnitude0
ClinVar
Risk rs273585626(T;T)
Alt rs273585626(T;T)
Reference rs273585626(C;C)
Significance Pathogenic
Disease Keratoconus 1
Variation info
Gene ZNF469
CLNDBN Keratoconus 1
Reversed 0
HGVS NC_000016.9:g.88503009C>T
CLNSRC ClinVar
CLNACC RCV000114789.1,