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rs764139968

From SNPedia

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Geno Mag Summary
(C;C) 0 common in clinvar
Make rs764139968(C;G)
Make rs764139968(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position88436738
GeneZNF469
is asnp
is mentioned by
dbSNPrs764139968
ebirs764139968
HLIrs764139968
Exacrs764139968
Varsomers764139968
Maprs764139968
PheGenIrs764139968
hapmaprs764139968
1000 genomesrs764139968
hgdprs764139968
ensemblrs764139968
gopubmedrs764139968
geneviewrs764139968
scholarrs764139968
googlers764139968
pharmgkbrs764139968
gwascentralrs764139968
openSNPrs764139968
23andMers764139968
23andMe allrs764139968
SNP Nexus

SNPshotrs764139968
SNPdbers764139968
MSV3drs764139968
GWAS Ctlgrs764139968
Max Magnitude0
ClinVar
Risk rs764139968(G;G)
Alt rs764139968(G;G)
Reference rs764139968(C;C)
Significance Pathogenic
Disease Corneal fragility keratoglobus
Variation info
Gene ZNF469
CLNDBN Corneal fragility keratoglobus, blue sclerae AND joint hypermobility
Reversed 0
HGVS NC_000016.9:g.88503146C>T
CLNSRC
CLNACC RCV000175661.1,