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rs28940281

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs28940281(C;T)
Make rs28940281(T;T)
ReferenceGRCh38 38.1/141
Chromosome8
Position1882669
GeneARHGEF10
is asnp
is mentioned by
dbSNPrs28940281
ebirs28940281
HLIrs28940281
Exacrs28940281
Varsomers28940281
Maprs28940281
PheGenIrs28940281
hapmaprs28940281
1000 genomesrs28940281
hgdprs28940281
ensemblrs28940281
gopubmedrs28940281
geneviewrs28940281
scholarrs28940281
googlers28940281
pharmgkbrs28940281
gwascentralrs28940281
openSNPrs28940281
23andMers28940281
23andMe allrs28940281
SNP Nexus

SNPshotrs28940281
SNPdbers28940281
MSV3drs28940281
GWAS Ctlgrs28940281
Max Magnitude0
OMIM608136
DescSLOWED NERVE CONDUCTION VELOCITY, AUTOSOMAL DOMINANT
Variant0001
Relatedalso


ClinVar
Risk rs28940281(T;T)
Alt rs28940281(T;T)
Reference rs28940281(C;C)
Significance Pathogenic
Disease Slowed nerve conduction velocity
Variation info
Gene ARHGEF10
CLNDBN Slowed nerve conduction velocity, autosomal dominant
Reversed 0
HGVS NC_000008.10:g.1830835C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000002634.4,