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rs28929768

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0
(T;T) 0 common in clinvar
Make rs28929768(C;C)
Make rs28929768(C;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position4902268
GeneCHRNE, C17orf107
is asnp
is mentioned by
dbSNPrs28929768
ebirs28929768
HLIrs28929768
Exacrs28929768
Varsomers28929768
Maprs28929768
PheGenIrs28929768
hapmaprs28929768
1000 genomesrs28929768
hgdprs28929768
ensemblrs28929768
gopubmedrs28929768
geneviewrs28929768
scholarrs28929768
googlers28929768
pharmgkbrs28929768
gwascentralrs28929768
openSNPrs28929768
23andMers28929768
23andMe allrs28929768
SNP Nexus

SNPshotrs28929768
SNPdbers28929768
MSV3drs28929768
GWAS Ctlgrs28929768
Max Magnitude0
OMIM100725
DescMYASTHENIC SYNDROME, SLOW-CHANNEL CONGENITAL, AUTOSOMAL RECESSIVE
Variant0009
Relatedalso


ClinVar
Risk rs28929768(C;C)
Alt rs28929768(C;C)
Reference rs28929768(T;T)
Significance Untested
Disease
Variation info
Gene C17orf107 CHRNE
CLNDBN
Reversed 1
HGVS NC_000017.10:g.4805563A>G
CLNSRC
CLNACC