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rs398124286

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(CAGA;CAGA) 0 common in clinvar
Make rs398124286(-;-)
Make rs398124286(-;CAGA)
ReferenceGRCh38 38.1/141
Chromosome9
Position132277144
GeneSETX
is asnp
is mentioned by
dbSNPrs398124286
ebirs398124286
HLIrs398124286
Exacrs398124286
Varsomers398124286
Maprs398124286
PheGenIrs398124286
hapmaprs398124286
1000 genomesrs398124286
hgdprs398124286
ensemblrs398124286
gopubmedrs398124286
geneviewrs398124286
scholarrs398124286
googlers398124286
pharmgkbrs398124286
gwascentralrs398124286
openSNPrs398124286
23andMers398124286
23andMe allrs398124286
SNP Nexus

SNPshotrs398124286
SNPdbers398124286
MSV3drs398124286
GWAS Ctlgrs398124286
Max Magnitude0
ClinVar
Risk rs398124286(;)
Alt rs398124286(;)
Reference rs398124286(CAGA;CAGA)
Significance Pathogenic
Disease not provided Amyotrophic lateral sclerosis type 4
Variation info
Gene SETX
CLNDBN not provided Amyotrophic lateral sclerosis type 4
Reversed 1
HGVS NC_000009.11:g.135152531_135152534delTCTG
CLNSRC HGMD
CLNACC RCV000081701.3, RCV000176318.1,