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

rs273585616

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs273585616(C;C)
Make rs273585616(C;G)
ReferenceGRCh38 38.1/142
Chromosome16
Position88427547
GeneZNF469
is asnp
is mentioned by
dbSNPrs273585616
ebirs273585616
HLIrs273585616
Exacrs273585616
Varsomers273585616
Maprs273585616
PheGenIrs273585616
hapmaprs273585616
1000 genomesrs273585616
hgdprs273585616
ensemblrs273585616
gopubmedrs273585616
geneviewrs273585616
scholarrs273585616
googlers273585616
pharmgkbrs273585616
gwascentralrs273585616
openSNPrs273585616
23andMers273585616
23andMe allrs273585616
SNP Nexus

SNPshotrs273585616
SNPdbers273585616
MSV3drs273585616
GWAS Ctlgrs273585616
Max Magnitude0
ClinVar
Risk rs273585616(C;C)
Alt rs273585616(C;C)
Reference rs273585616(G;G)
Significance Pathogenic
Disease Keratoconus 1
Variation info
Gene ZNF469
CLNDBN Keratoconus 1
Reversed 0
HGVS NC_000016.9:g.88493955G>C
CLNSRC ClinVar
CLNACC RCV000114787.1,