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rs587781249

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587781249(-;-)
Make rs587781249(-;TGA)
Make rs587781249(TGA;TGA)
ReferenceGRCh38.p2 38.2/144
Chromosome9
Position132328522
GeneSETX
is asnp
is mentioned by
dbSNPrs587781249
ebirs587781249
HLIrs587781249
Exacrs587781249
Varsomers587781249
Maprs587781249
PheGenIrs587781249
hapmaprs587781249
1000 genomesrs587781249
hgdprs587781249
ensemblrs587781249
gopubmedrs587781249
geneviewrs587781249
scholarrs587781249
googlers587781249
pharmgkbrs587781249
gwascentralrs587781249
openSNPrs587781249
23andMers587781249
23andMe allrs587781249
SNP Nexus

SNPshotrs587781249
SNPdbers587781249
MSV3drs587781249
GWAS Ctlgrs587781249
Max Magnitude0
ClinVar
Risk rs587781249(TGA;TGA)
Alt rs587781249(TGA;TGA)
Reference rs587781249(;)
Significance Probable-Pathogenic
Disease Charcot-Marie-Tooth disease
Variation info
Gene SETX
CLNDBN Charcot-Marie-Tooth disease
Reversed 1
HGVS NC_000009.11:g.135203909_135203910insTCA
CLNSRC
CLNACC RCV000144873.1,