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rs281865152

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs281865152(A;A)
Make rs281865152(A;G)
ReferenceGRCh38 38.1/142
Chromosome16
Position88435401
GeneZNF469
is asnp
is mentioned by
dbSNPrs281865152
ebirs281865152
HLIrs281865152
Exacrs281865152
Varsomers281865152
Maprs281865152
PheGenIrs281865152
hapmaprs281865152
1000 genomesrs281865152
hgdprs281865152
ensemblrs281865152
gopubmedrs281865152
geneviewrs281865152
scholarrs281865152
googlers281865152
pharmgkbrs281865152
gwascentralrs281865152
openSNPrs281865152
23andMers281865152
23andMe allrs281865152
SNP Nexus

SNPshotrs281865152
SNPdbers281865152
MSV3drs281865152
GWAS Ctlgrs281865152
Max Magnitude0
ClinVar
Risk rs281865152(A;A)
Alt rs281865152(A;A)
Reference rs281865152(G;G)
Significance Probable-Pathogenic
Disease Keratoconus 1
Variation info
Gene ZNF469
CLNDBN Keratoconus 1
Reversed 0
HGVS NC_000016.9:g.88501809G>A
CLNSRC ClinVar
CLNACC RCV000114802.1,