rs1149374

Orientation

plus

Stabilized

plus

Make rs1149374(A;A)

Make rs1149374(A;C)

Make rs1149374(C;C)

Reference

GRCh38 38.1/141

Chromosome

X

Position

151221459

is a	snp
is	mentioned by
dbSNP	rs1149374
dbSNP (classic)	rs1149374
ClinGen	rs1149374
ebi	rs1149374
HLI	rs1149374
Exac	rs1149374
Gnomad	rs1149374
Varsome	rs1149374
LitVar	rs1149374
Map	rs1149374
PheGenI	rs1149374
Biobank	rs1149374
1000 genomes	rs1149374
hgdp	rs1149374
ensembl	rs1149374
geneview	rs1149374
scholar	rs1149374
google	rs1149374
pharmgkb	rs1149374
gwascentral	rs1149374
openSNP	rs1149374
23andMe	rs1149374
SNPshot	rs1149374
SNPdbe	rs1149374
MSV3d	rs1149374
GWAS Ctlg	rs1149374

GMAF

0.2811

Max Magnitude

0

?	(A;A) (A;C) (C;C)	28

OMIM	310440
Desc	MYOPATHY, X-LINKED, WITH EXCESSIVE AUTOPHAGY; MEAX
Variant
Related	also