rs1599711

Orientation

minus

Stabilized

minus

Make rs1599711(C;C)

Make rs1599711(C;T)

Make rs1599711(T;T)

Reference

GRCh38 38.1/142

Chromosome

10

Position

69611373

is a	snp
is	mentioned by
dbSNP	rs1599711
dbSNP (classic)	rs1599711
ClinGen	rs1599711
ebi	rs1599711
HLI	rs1599711
Exac	rs1599711
Gnomad	rs1599711
Varsome	rs1599711
LitVar	rs1599711
Map	rs1599711
PheGenI	rs1599711
Biobank	rs1599711
1000 genomes	rs1599711
hgdp	rs1599711
ensembl	rs1599711
geneview	rs1599711
scholar	rs1599711
google	rs1599711
pharmgkb	rs1599711
gwascentral	rs1599711
openSNP	rs1599711
23andMe	rs1599711
SNPshot	rs1599711
SNPdbe	rs1599711
MSV3d	rs1599711
GWAS Ctlg	rs1599711

GMAF

0.2539

Max Magnitude

0

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

OMIM	611094
Desc	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 8; MRT8
Variant
Related	also