rs794726690

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(-;-)	0	common in clinvar

Make rs794726690(-;G)

Make rs794726690(G;G)

Reference

GRCh38.p2 38.2/146

Chromosome

1

Position

150558037

Gene	ADAMTSL4, LOC100289061

is a	snp
is	mentioned by
dbSNP	rs794726690
dbSNP (classic)	rs794726690
ClinGen	rs794726690
ebi	rs794726690
HLI	rs794726690
Exac	rs794726690
Gnomad	rs794726690
Varsome	rs794726690
LitVar	rs794726690
Map	rs794726690
PheGenI	rs794726690
Biobank	rs794726690
1000 genomes	rs794726690
hgdp	rs794726690
ensembl	rs794726690
geneview	rs794726690
scholar	rs794726690
google	rs794726690
pharmgkb	rs794726690
gwascentral	rs794726690
openSNP	rs794726690
23andMe	rs794726690
SNPshot	rs794726690
SNPdbe	rs794726690
MSV3d	rs794726690
GWAS Ctlg	rs794726690

Max Magnitude

0

ClinVar
Risk	rs794726690(G;G)
Alt	rs794726690(G;G)
Reference	Rs794726690(-;-)
Significance	Pathogenic
Disease	Ectopia lentis et pupillae not provided
Variation	info
Gene	ADAMTSL4
CLNDBN	Ectopia lentis et pupillae not provided
Reversed	0
HGVS	NC_000001.10:g.150530513dupG
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000032759.4, RCV000485448.1,