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rs794726690

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs794726690(-;-)
Make rs794726690(-;G)
Make rs794726690(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position150558037
GeneADAMTSL4, LOC100289061
is asnp
is mentioned by
dbSNPrs794726690
ebirs794726690
HLIrs794726690
Exacrs794726690
Varsomers794726690
Maprs794726690
PheGenIrs794726690
hapmaprs794726690
1000 genomesrs794726690
hgdprs794726690
ensemblrs794726690
gopubmedrs794726690
geneviewrs794726690
scholarrs794726690
googlers794726690
pharmgkbrs794726690
gwascentralrs794726690
openSNPrs794726690
23andMers794726690
23andMe allrs794726690
SNP Nexus

SNPshotrs794726690
SNPdbers794726690
MSV3drs794726690
GWAS Ctlgrs794726690
Max Magnitude0
ClinVar
Risk rs794726690(G;G)
Alt rs794726690(G;G)
Reference rs794726690(;)
Significance Pathogenic
Disease Ectopia lentis et pupillae
Variation info
Gene ADAMTSL4
CLNDBN Ectopia lentis et pupillae
Reversed 0
HGVS NC_000001.10:g.150530513dupG
CLNSRC OMIM Allelic Variant
CLNACC RCV000032759.4,