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rs281865150

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs281865150(A;T)
Make rs281865150(T;T)
ReferenceGRCh38 38.1/142
Chromosome16
Position88433151
GeneZNF469
is asnp
is mentioned by
dbSNPrs281865150
ebirs281865150
HLIrs281865150
Exacrs281865150
Varsomers281865150
Maprs281865150
PheGenIrs281865150
hapmaprs281865150
1000 genomesrs281865150
hgdprs281865150
ensemblrs281865150
gopubmedrs281865150
geneviewrs281865150
scholarrs281865150
googlers281865150
pharmgkbrs281865150
gwascentralrs281865150
openSNPrs281865150
23andMers281865150
23andMe allrs281865150
SNP Nexus

SNPshotrs281865150
SNPdbers281865150
MSV3drs281865150
GWAS Ctlgrs281865150
Max Magnitude0
ClinVar
Risk rs281865150(T;T)
Alt rs281865150(T;T)
Reference rs281865150(A;A)
Significance Pathogenic
Disease Keratoconus 1
Variation info
Gene ZNF469
CLNDBN Keratoconus 1
Reversed 0
HGVS NC_000016.9:g.88499559A>T
CLNSRC ClinVar
CLNACC RCV000114800.1,