Have questions? Visit https://www.reddit.com/r/SNPedia

rs281865146

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs281865146(A;A)
Make rs281865146(A;C)
ReferenceGRCh38 38.1/142
Chromosome16
Position88429533
GeneZNF469
is asnp
is mentioned by
dbSNPrs281865146
ebirs281865146
HLIrs281865146
Exacrs281865146
Varsomers281865146
Maprs281865146
PheGenIrs281865146
hapmaprs281865146
1000 genomesrs281865146
hgdprs281865146
ensemblrs281865146
gopubmedrs281865146
geneviewrs281865146
scholarrs281865146
googlers281865146
pharmgkbrs281865146
gwascentralrs281865146
openSNPrs281865146
23andMers281865146
23andMe allrs281865146
SNP Nexus

SNPshotrs281865146
SNPdbers281865146
MSV3drs281865146
GWAS Ctlgrs281865146
Max Magnitude0
ClinVar
Risk rs281865146(A;A)
Alt rs281865146(A;A)
Reference rs281865146(C;C)
Significance Pathogenic
Disease Keratoconus 1
Variation info
Gene ZNF469
CLNDBN Keratoconus 1
Reversed 0
HGVS NC_000016.9:g.88495941C>A
CLNSRC ClinVar
CLNACC RCV000114794.1,