rs1824938

Orientation

minus

Stabilized

minus

Make rs1824938(C;C)

Make rs1824938(C;T)

Make rs1824938(T;T)

Reference

GRCh38 38.1/141

Chromosome

5

Position

5091915

is a	snp
is	mentioned by
dbSNP	rs1824938
dbSNP (classic)	rs1824938
ClinGen	rs1824938
ebi	rs1824938
HLI	rs1824938
Exac	rs1824938
Gnomad	rs1824938
Varsome	rs1824938
LitVar	rs1824938
Map	rs1824938
PheGenI	rs1824938
Biobank	rs1824938
1000 genomes	rs1824938
hgdp	rs1824938
ensembl	rs1824938
geneview	rs1824938
scholar	rs1824938
google	rs1824938
pharmgkb	rs1824938
gwascentral	rs1824938
openSNP	rs1824938
23andMe	rs1824938
SNPshot	rs1824938
SNPdbe	rs1824938
MSV3d	rs1824938
GWAS Ctlg	rs1824938

GMAF

0.2516

Max Magnitude

0

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

OMIM	611091
Desc	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 5; MRT5
Variant
Related	also

[PMID 17903302] Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness.