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rs273585632

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs273585632(A;A)
Make rs273585632(A;G)
ReferenceGRCh38 38.1/142
Chromosome16
Position88428190
GeneZNF469
is asnp
is mentioned by
dbSNPrs273585632
ebirs273585632
HLIrs273585632
Exacrs273585632
Varsomers273585632
Maprs273585632
PheGenIrs273585632
hapmaprs273585632
1000 genomesrs273585632
hgdprs273585632
ensemblrs273585632
gopubmedrs273585632
geneviewrs273585632
scholarrs273585632
googlers273585632
pharmgkbrs273585632
gwascentralrs273585632
openSNPrs273585632
23andMers273585632
23andMe allrs273585632
SNP Nexus

SNPshotrs273585632
SNPdbers273585632
MSV3drs273585632
GWAS Ctlgrs273585632
Max Magnitude0
ClinVar
Risk rs273585632(A;A)
Alt rs273585632(A;A)
Reference rs273585632(G;G)
Significance Probable-Pathogenic
Disease Keratoconus 1
Variation info
Gene ZNF469
CLNDBN Keratoconus 1
Reversed 0
HGVS NC_000016.9:g.88494598G>A
CLNSRC ClinVar
CLNACC RCV000114786.1,