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rs387907109

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs387907109(A;G)
Make rs387907109(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position90939340
GeneZNF644
is asnp
is mentioned by
dbSNPrs387907109
ebirs387907109
HLIrs387907109
Exacrs387907109
Varsomers387907109
Maprs387907109
PheGenIrs387907109
hapmaprs387907109
1000 genomesrs387907109
hgdprs387907109
ensemblrs387907109
gopubmedrs387907109
geneviewrs387907109
scholarrs387907109
googlers387907109
pharmgkbrs387907109
gwascentralrs387907109
openSNPrs387907109
23andMers387907109
23andMe allrs387907109
SNP Nexus

SNPshotrs387907109
SNPdbers387907109
MSV3drs387907109
GWAS Ctlgrs387907109
Max Magnitude0
ClinVar
Risk rs387907109(G;G)
Alt rs387907109(G;G)
Reference rs387907109(A;A)
Significance Pathogenic
Disease Myopia 21
Variation info
Gene ZNF644
CLNDBN Myopia 21, autosomal dominant
Reversed 1
HGVS NC_000001.10:g.91404897T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000024103.2,