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rs869320629

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs869320629(C;C)
Make rs869320629(C;T)
ReferenceGRCh38.p2 38.2/147
Chromosome20
Position18057941
GeneOVOL2
is asnp
is mentioned by
dbSNPrs869320629
ebirs869320629
HLIrs869320629
Exacrs869320629
Varsomers869320629
Maprs869320629
PheGenIrs869320629
hapmaprs869320629
1000 genomesrs869320629
hgdprs869320629
ensemblrs869320629
gopubmedrs869320629
geneviewrs869320629
scholarrs869320629
googlers869320629
pharmgkbrs869320629
gwascentralrs869320629
openSNPrs869320629
23andMers869320629
23andMe allrs869320629
SNP Nexus

SNPshotrs869320629
SNPdbers869320629
MSV3drs869320629
GWAS Ctlgrs869320629
Max Magnitude0
ClinVar
Risk rs869320629(C;C)
Alt rs869320629(C;C)
Reference rs869320629(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.18038585A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000210427.1,