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rs273585627

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs273585627(A;G)
Make rs273585627(G;G)
ReferenceGRCh38 38.1/142
Chromosome16
Position88437389
GeneZNF469
is asnp
is mentioned by
dbSNPrs273585627
ebirs273585627
HLIrs273585627
Exacrs273585627
Varsomers273585627
Maprs273585627
PheGenIrs273585627
hapmaprs273585627
1000 genomesrs273585627
hgdprs273585627
ensemblrs273585627
gopubmedrs273585627
geneviewrs273585627
scholarrs273585627
googlers273585627
pharmgkbrs273585627
gwascentralrs273585627
openSNPrs273585627
23andMers273585627
23andMe allrs273585627
SNP Nexus

SNPshotrs273585627
SNPdbers273585627
MSV3drs273585627
GWAS Ctlgrs273585627
Max Magnitude0
ClinVar
Risk rs273585627(G;G)
Alt rs273585627(G;G)
Reference rs273585627(A;A)
Significance Probable-Pathogenic
Disease Keratoconus 1
Variation info
Gene ZNF469
CLNDBN Keratoconus 1
Reversed 0
HGVS NC_000016.9:g.88503797A>G
CLNSRC ClinVar
CLNACC RCV000114791.1,