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rs863224866

From SNPedia

Orientationplus
Make rs863224866(-;-)
Make rs863224866(-;C)
ReferenceGRCh38.p2 38.2/146
Chromosome4
Position3493249
GeneDOK7
is asnp
is mentioned by
dbSNPrs863224866
ClinGenrs863224866
ebirs863224866
HLIrs863224866
Exacrs863224866
Varsomers863224866
Maprs863224866
PheGenIrs863224866
hapmaprs863224866
1000 genomesrs863224866
hgdprs863224866
ensemblrs863224866
gopubmedrs863224866
geneviewrs863224866
scholarrs863224866
googlers863224866
pharmgkbrs863224866
gwascentralrs863224866
openSNPrs863224866
23andMers863224866
23andMe allrs863224866
SNP Nexus

SNPshotrs863224866
SNPdbers863224866
MSV3drs863224866
GWAS Ctlgrs863224866
Max Magnitude
ClinVar
Risk
Alt
Reference Rs863224866(C;C)
Significance Probable-Pathogenic
Disease Myasthenia
Variation info
Gene DOK7
CLNDBN Myasthenia, limb-girdle, familial
Reversed 0
HGVS NC_000004.11:g.3494976delC
CLNSRC
CLNACC RCV000200829.1,