rs1057519019

Orientation

minus

Stabilized

minus

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

Make rs1057519019(A;A)

Make rs1057519019(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

15

Position

100573936

Gene

LINS1

is a	snp
is	mentioned by
dbSNP	rs1057519019
dbSNP (classic)	rs1057519019
ClinGen	rs1057519019
ebi	rs1057519019
HLI	rs1057519019
Exac	rs1057519019
Gnomad	rs1057519019
Varsome	rs1057519019
LitVar	rs1057519019
Map	rs1057519019
PheGenI	rs1057519019
Biobank	rs1057519019
1000 genomes	rs1057519019
hgdp	rs1057519019
ensembl	rs1057519019
geneview	rs1057519019
scholar	rs1057519019
google	rs1057519019
pharmgkb	rs1057519019
gwascentral	rs1057519019
openSNP	rs1057519019
23andMe	rs1057519019
SNPshot	rs1057519019
SNPdbe	rs1057519019
MSV3d	rs1057519019
GWAS Ctlg	rs1057519019

Max Magnitude

0

ClinVar
Risk	rs1057519019(A;A)
Alt	rs1057519019(A;A)
Reference	Rs1057519019(G;G)
Significance	Probable-Pathogenic
Disease	Mental retardation
Variation	info
Gene	LINS LINS1
CLNDBN	Mental retardation, autosomal recessive 27
Reversed	1
HGVS	NC_000015.9:g.101114141C>T
CLNSRC
CLNACC	RCV000415720.1,