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rs28929482

From SNPedia

Merged intors75466054
Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0
Make rs28929482(C;C)
Make rs28929482(C;T)
ReferenceGRCh38 38.1/141
Chromosome10
Position49625634
GeneCHAT
is asnp
is mentioned by
dbSNPrs28929482
ebirs28929482
HLIrs28929482
Exacrs28929482
Varsomers28929482
Maprs28929482
PheGenIrs28929482
hapmaprs28929482
1000 genomesrs28929482
hgdprs28929482
ensemblrs28929482
gopubmedrs28929482
geneviewrs28929482
scholarrs28929482
googlers28929482
pharmgkbrs28929482
gwascentralrs28929482
openSNPrs28929482
23andMers28929482
23andMe allrs28929482
SNP Nexus

SNPshotrs28929482
SNPdbers28929482
MSV3drs28929482
GWAS Ctlgrs28929482
StatusMerged into rs75466054
Max Magnitude0
OMIM118490
DescMYASTHENIC SYNDROME, CONGENITAL, ASSOCIATED WITH EPISODIC APNEA
Variant0009
Relatedalso