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rs761899995

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs761899995(-;-)
Make rs761899995(-;G)
ReferenceGRCh38.p2 38.2/146
Chromosome4
Position3493124
GeneDOK7
is asnp
is mentioned by
dbSNPrs761899995
ebirs761899995
HLIrs761899995
Exacrs761899995
Varsomers761899995
Maprs761899995
PheGenIrs761899995
hapmaprs761899995
1000 genomesrs761899995
hgdprs761899995
ensemblrs761899995
gopubmedrs761899995
geneviewrs761899995
scholarrs761899995
googlers761899995
pharmgkbrs761899995
gwascentralrs761899995
openSNPrs761899995
23andMers761899995
23andMe allrs761899995
SNP Nexus

SNPshotrs761899995
SNPdbers761899995
MSV3drs761899995
GWAS Ctlgrs761899995
Max Magnitude0
ClinVar
Risk rs761899995(GC,GG;GC,GG)
Alt rs761899995(GC,GG;GC,GG)
Reference rs761899995(G;G)
Significance Pathogenic
Disease Myasthenia
Variation info
Gene DOK7
CLNDBN Myasthenia, limb-girdle, familial
Reversed 0
HGVS NC_000004.11:g.3494851dupG
CLNSRC Baylor College of Medicine
CLNACC RCV000191080.1,