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rs273585634

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs273585634(G;T)
Make rs273585634(T;T)
ReferenceGRCh38 38.1/142
Chromosome16
Position88429948
GeneZNF469
is asnp
is mentioned by
dbSNPrs273585634
ebirs273585634
HLIrs273585634
Exacrs273585634
Varsomers273585634
Maprs273585634
PheGenIrs273585634
hapmaprs273585634
1000 genomesrs273585634
hgdprs273585634
ensemblrs273585634
gopubmedrs273585634
geneviewrs273585634
scholarrs273585634
googlers273585634
pharmgkbrs273585634
gwascentralrs273585634
openSNPrs273585634
23andMers273585634
23andMe allrs273585634
SNP Nexus

SNPshotrs273585634
SNPdbers273585634
MSV3drs273585634
GWAS Ctlgrs273585634
Max Magnitude0
ClinVar
Risk rs273585634(T;T)
Alt rs273585634(T;T)
Reference rs273585634(G;G)
Significance Probable-Pathogenic
Disease Keratoconus 1
Variation info
Gene ZNF469
CLNDBN Keratoconus 1
Reversed 0
HGVS NC_000016.9:g.88496356G>T
CLNSRC ClinVar
CLNACC RCV000114776.1,