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rs753021890

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs753021890(A;A)
Make rs753021890(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome9
Position27168578
GeneTEK
is asnp
is mentioned by
dbSNPrs753021890
dbSNP (old)rs753021890
ClinGenrs753021890
ebirs753021890
HLIrs753021890
Exacrs753021890
Varsomers753021890
Maprs753021890
PheGenIrs753021890
Biobankrs753021890
1000 genomesrs753021890
hgdprs753021890
ensemblrs753021890
gopubmedrs753021890
geneviewrs753021890
scholarrs753021890
googlers753021890
pharmgkbrs753021890
gwascentralrs753021890
openSNPrs753021890
23andMers753021890
23andMe allrs753021890
SNP Nexus

SNPshotrs753021890
SNPdbers753021890
MSV3drs753021890
GWAS Ctlgrs753021890
Max Magnitude0
ClinVar
Risk rs753021890(A;A) rs753021890(T;T)
Alt rs753021890(A;A) rs753021890(T;T)
Reference Rs753021890(G;G)
Significance Pathogenic
Disease Glaucoma 3
Variation info
Gene TEK
CLNDBN Glaucoma 3, primary congenital, E
Reversed 0
HGVS NC_000009.11:g.27168576G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000415600.1,