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rs4743056

From SNPedia

Orientationplus
Stabilizedplus
Make rs4743056(C;C)
Make rs4743056(C;T)
Make rs4743056(T;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position97059329
is asnp
is mentioned by
dbSNPrs4743056
ebirs4743056
HLIrs4743056
Exacrs4743056
Varsomers4743056
Maprs4743056
PheGenIrs4743056
hapmaprs4743056
1000 genomesrs4743056
hgdprs4743056
ensemblrs4743056
gopubmedrs4743056
geneviewrs4743056
scholarrs4743056
googlers4743056
pharmgkbrs4743056
gwascentralrs4743056
openSNPrs4743056
23andMers4743056
23andMe allrs4743056
SNP Nexus

SNPshotrs4743056
SNPdbers4743056
MSV3drs4743056
GWAS Ctlgrs4743056
GMAF0.494
Max Magnitude
? (C;C) (C;T) (T;T) 28
rs4743056 increases susceptibility to Myasthenia gravis 1.37 times for carriers of the G allele [PMID 17869649]

rs4743056 increases susceptibility to Myasthenia gravis, early onset 1.61 times for carriers of the G allele [PMID 17869649]