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rs1149374

From SNPedia

Orientationplus
Stabilizedplus
Make rs1149374(A;A)
Make rs1149374(A;C)
Make rs1149374(C;C)
ReferenceGRCh38 38.1/141
ChromosomeX
Position151221459
is asnp
is mentioned by
dbSNPrs1149374
ebirs1149374
HLIrs1149374
Exacrs1149374
Varsomers1149374
Maprs1149374
PheGenIrs1149374
hapmaprs1149374
1000 genomesrs1149374
hgdprs1149374
ensemblrs1149374
gopubmedrs1149374
geneviewrs1149374
scholarrs1149374
googlers1149374
pharmgkbrs1149374
gwascentralrs1149374
openSNPrs1149374
23andMers1149374
23andMe allrs1149374
SNP Nexus

SNPshotrs1149374
SNPdbers1149374
MSV3drs1149374
GWAS Ctlgrs1149374
GMAF0.2811
Max Magnitude
? (A;A) (A;C) (C;C) 28
OMIM310440
DescMYOPATHY, X-LINKED, WITH EXCESSIVE AUTOPHAGY; MEAX
Variant
Relatedalso