rs1998463

Orientation

plus

Stabilized

plus

Make rs1998463(C;C)

Make rs1998463(C;G)

Make rs1998463(G;G)

Reference

GRCh38 38.1/141

Chromosome

14

Position

27039812

is a	snp
is	mentioned by
dbSNP	rs1998463
dbSNP (classic)	rs1998463
ClinGen	rs1998463
ebi	rs1998463
HLI	rs1998463
Exac	rs1998463
Gnomad	rs1998463
Varsome	rs1998463
LitVar	rs1998463
Map	rs1998463
PheGenI	rs1998463
Biobank	rs1998463
1000 genomes	rs1998463
hgdp	rs1998463
ensembl	rs1998463
geneview	rs1998463
scholar	rs1998463
google	rs1998463
pharmgkb	rs1998463
gwascentral	rs1998463
openSNP	rs1998463
23andMe	rs1998463
SNPshot	rs1998463
SNPdbe	rs1998463
MSV3d	rs1998463
GWAS Ctlg	rs1998463

GMAF

0.3375

Max Magnitude

0

?	(C;C) (C;G) (G;G)	28

OMIM	611095
Desc	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 9; MRT9
Variant
Related	also