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rs273585620

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs273585620(G;T)
Make rs273585620(T;T)
ReferenceGRCh38 38.1/142
Chromosome16
Position88431917
GeneZNF469
is asnp
is mentioned by
dbSNPrs273585620
ebirs273585620
HLIrs273585620
Exacrs273585620
Varsomers273585620
Maprs273585620
PheGenIrs273585620
hapmaprs273585620
1000 genomesrs273585620
hgdprs273585620
ensemblrs273585620
gopubmedrs273585620
geneviewrs273585620
scholarrs273585620
googlers273585620
pharmgkbrs273585620
gwascentralrs273585620
openSNPrs273585620
23andMers273585620
23andMe allrs273585620
SNP Nexus

SNPshotrs273585620
SNPdbers273585620
MSV3drs273585620
GWAS Ctlgrs273585620
Max Magnitude0
ClinVar
Risk rs273585620(T;T)
Alt rs273585620(T;T)
Reference rs273585620(G;G)
Significance Pathogenic
Disease Keratoconus 1
Variation info
Gene ZNF469
CLNDBN Keratoconus 1
Reversed 0
HGVS NC_000016.9:g.88498325G>T
CLNSRC ClinVar
CLNACC RCV000114781.1,