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rs869320628

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs869320628(C;C)
Make rs869320628(C;T)
ReferenceGRCh38.p2 38.2/147
Chromosome20
Position18058004
GeneOVOL2
is asnp
is mentioned by
dbSNPrs869320628
ebirs869320628
HLIrs869320628
Exacrs869320628
Varsomers869320628
Maprs869320628
PheGenIrs869320628
hapmaprs869320628
1000 genomesrs869320628
hgdprs869320628
ensemblrs869320628
gopubmedrs869320628
geneviewrs869320628
scholarrs869320628
googlers869320628
pharmgkbrs869320628
gwascentralrs869320628
openSNPrs869320628
23andMers869320628
23andMe allrs869320628
SNP Nexus

SNPshotrs869320628
SNPdbers869320628
MSV3drs869320628
GWAS Ctlgrs869320628
Max Magnitude0
ClinVar
Risk rs869320628(C;C)
Alt rs869320628(C;C)
Reference rs869320628(T;T)
Significance Pathogenic
Disease Posterior polymorphous corneal dystrophy 1
Variation info
Gene OVOL2
CLNDBN Posterior polymorphous corneal dystrophy 1
Reversed 1
HGVS NC_000020.10:g.18038648A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000210419.1,