rs724466

Orientation

minus

Stabilized

minus

Make rs724466(C;C)

Make rs724466(C;T)

Make rs724466(T;T)

Reference

GRCh38 38.1/141

Chromosome

16

Position

22786531

is a	snp
is	mentioned by
dbSNP	rs724466
dbSNP (classic)	rs724466
ClinGen	rs724466
ebi	rs724466
HLI	rs724466
Exac	rs724466
Gnomad	rs724466
Varsome	rs724466
LitVar	rs724466
Map	rs724466
PheGenI	rs724466
Biobank	rs724466
1000 genomes	rs724466
hgdp	rs724466
ensembl	rs724466
geneview	rs724466
scholar	rs724466
google	rs724466
pharmgkb	rs724466
gwascentral	rs724466
openSNP	rs724466
23andMe	rs724466
SNPshot	rs724466
SNPdbe	rs724466
MSV3d	rs724466
GWAS Ctlg	rs724466

GMAF

0.2847

Max Magnitude

0

?	(C;C) (C;T) (T;T)	28

OMIM	611096
Desc	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 10; MRT10
Variant
Related	also