rs606231459

Orientation

plus

Stabilized

plus

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

Make rs606231459(A;A)

Make rs606231459(A;G)

Reference

GRCh38.p2 38.2/144

Chromosome

5

Position

150541651

Gene

NDST1

is a	snp
is	mentioned by
dbSNP	rs606231459
dbSNP (classic)	rs606231459
ClinGen	rs606231459
ebi	rs606231459
HLI	rs606231459
Exac	rs606231459
Gnomad	rs606231459
Varsome	rs606231459
LitVar	rs606231459
Map	rs606231459
PheGenI	rs606231459
Biobank	rs606231459
1000 genomes	rs606231459
hgdp	rs606231459
ensembl	rs606231459
geneview	rs606231459
scholar	rs606231459
google	rs606231459
pharmgkb	rs606231459
gwascentral	rs606231459
openSNP	rs606231459
23andMe	rs606231459
SNPshot	rs606231459
SNPdbe	rs606231459
MSV3d	rs606231459
GWAS Ctlg	rs606231459

Max Magnitude

0

ClinVar
Risk	rs606231459(A;A)
Alt	rs606231459(A;A)
Reference	Rs606231459(G;G)
Significance	Pathogenic
Disease	Mental retardation
Variation	info
Gene	NDST1
CLNDBN	Mental retardation, autosomal recessive 46
Reversed	0
HGVS	NC_000005.9:g.149921213G>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000148928.6,