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rs369535598

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs369535598(A;A)
Make rs369535598(A;G)
ReferenceGRCh38 38.1/142
Chromosome2
Position1666484
GenePXDN
is asnp
is mentioned by
dbSNPrs369535598
ebirs369535598
HLIrs369535598
Exacrs369535598
Varsomers369535598
Maprs369535598
PheGenIrs369535598
hapmaprs369535598
1000 genomesrs369535598
hgdprs369535598
ensemblrs369535598
gopubmedrs369535598
geneviewrs369535598
scholarrs369535598
googlers369535598
pharmgkbrs369535598
gwascentralrs369535598
openSNPrs369535598
23andMers369535598
23andMe allrs369535598
SNP Nexus

SNPshotrs369535598
SNPdbers369535598
MSV3drs369535598
GWAS Ctlgrs369535598
Max Magnitude0
ClinVar
Risk rs369535598(A;A)
Alt rs369535598(A;A)
Reference rs369535598(G;G)
Significance Pathogenic
Disease Corneal opacification with other ocular anomalies
Variation info
Gene PXDN
CLNDBN Corneal opacification with other ocular anomalies
Reversed 0
HGVS NC_000002.11:g.1670256G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000128855.3,