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rs863225124

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863225124(G;T)
Make rs863225124(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position140676758
GeneHARS
is asnp
is mentioned by
dbSNPrs863225124
ebirs863225124
HLIrs863225124
Exacrs863225124
Varsomers863225124
Maprs863225124
PheGenIrs863225124
hapmaprs863225124
1000 genomesrs863225124
hgdprs863225124
ensemblrs863225124
gopubmedrs863225124
geneviewrs863225124
scholarrs863225124
googlers863225124
pharmgkbrs863225124
gwascentralrs863225124
openSNPrs863225124
23andMers863225124
23andMe allrs863225124
SNP Nexus

SNPshotrs863225124
SNPdbers863225124
MSV3drs863225124
GWAS Ctlgrs863225124
Max Magnitude0
ClinVar
Risk rs863225124(T;T)
Alt rs863225124(T;T)
Reference rs863225124(G;G)
Significance Pathogenic
Disease Charcot-Marie-Tooth disease
Variation info
Gene HARS
CLNDBN Charcot-Marie-Tooth disease, axonal, type 2w
Reversed 1
HGVS NC_000005.9:g.140056343C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000201523.1,