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rs281865151

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs281865151(A;A)
Make rs281865151(A;G)
ReferenceGRCh38 38.1/142
Chromosome16
Position88435301
GeneZNF469
is asnp
is mentioned by
dbSNPrs281865151
ebirs281865151
HLIrs281865151
Exacrs281865151
Varsomers281865151
Maprs281865151
PheGenIrs281865151
hapmaprs281865151
1000 genomesrs281865151
hgdprs281865151
ensemblrs281865151
gopubmedrs281865151
geneviewrs281865151
scholarrs281865151
googlers281865151
pharmgkbrs281865151
gwascentralrs281865151
openSNPrs281865151
23andMers281865151
23andMe allrs281865151
SNP Nexus

SNPshotrs281865151
SNPdbers281865151
MSV3drs281865151
GWAS Ctlgrs281865151
Max Magnitude0
ClinVar
Risk rs281865151(A;A)
Alt rs281865151(A;A)
Reference rs281865151(G;G)
Significance Probable-Pathogenic
Disease Keratoconus 1
Variation info
Gene ZNF469
CLNDBN Keratoconus 1
Reversed 0
HGVS NC_000016.9:g.88501709G>A
CLNSRC ClinVar
CLNACC RCV000114801.1,