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rs606231133

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs606231133(-;-)
Make rs606231133(-;C)
Make rs606231133(C;C)
ReferenceGRCh38.p2 38.2/144
Chromosome4
Position3493364
GeneDOK7
is asnp
is mentioned by
dbSNPrs606231133
ebirs606231133
HLIrs606231133
Exacrs606231133
Varsomers606231133
Maprs606231133
PheGenIrs606231133
hapmaprs606231133
1000 genomesrs606231133
hgdprs606231133
ensemblrs606231133
gopubmedrs606231133
geneviewrs606231133
scholarrs606231133
googlers606231133
pharmgkbrs606231133
gwascentralrs606231133
openSNPrs606231133
23andMers606231133
23andMe allrs606231133
SNP Nexus

SNPshotrs606231133
SNPdbers606231133
MSV3drs606231133
GWAS Ctlgrs606231133
Max Magnitude0
ClinVar
Risk rs606231133(C;C)
Alt rs606231133(C;C)
Reference rs606231133(;)
Significance Pathogenic
Disease Myasthenia
Variation info
Gene DOK7
CLNDBN Myasthenia, limb-girdle, familial
Reversed 0
HGVS NC_000004.11:g.3495091dupC
CLNSRC OMIM Allelic Variant
CLNACC RCV000001345.4,