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rs281865149

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs281865149(A;A)
Make rs281865149(A;G)
ReferenceGRCh38 38.1/142
Chromosome16
Position88432614
GeneZNF469
is asnp
is mentioned by
dbSNPrs281865149
ebirs281865149
HLIrs281865149
Exacrs281865149
Varsomers281865149
Maprs281865149
PheGenIrs281865149
hapmaprs281865149
1000 genomesrs281865149
hgdprs281865149
ensemblrs281865149
gopubmedrs281865149
geneviewrs281865149
scholarrs281865149
googlers281865149
pharmgkbrs281865149
gwascentralrs281865149
openSNPrs281865149
23andMers281865149
23andMe allrs281865149
SNP Nexus

SNPshotrs281865149
SNPdbers281865149
MSV3drs281865149
GWAS Ctlgrs281865149
Max Magnitude0
ClinVar
Risk rs281865149(A;A)
Alt rs281865149(A;A)
Reference rs281865149(G;G)
Significance Probable-Pathogenic
Disease Keratoconus 1
Variation info
Gene ZNF469
CLNDBN Keratoconus 1
Reversed 0
HGVS NC_000016.9:g.88499022G>A
CLNSRC ClinVar
CLNACC RCV000114799.1,