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rs1057520367

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057520367(C;T)
Make rs1057520367(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome9
Position132349406
GeneSETX
is asnp
is mentioned by
dbSNPrs1057520367
dbSNP (old)rs1057520367
ClinGenrs1057520367
ebirs1057520367
HLIrs1057520367
Exacrs1057520367
Gnomadrs1057520367
Varsomers1057520367
Maprs1057520367
PheGenIrs1057520367
Biobankrs1057520367
1000 genomesrs1057520367
hgdprs1057520367
ensemblrs1057520367
gopubmedrs1057520367
geneviewrs1057520367
scholarrs1057520367
googlers1057520367
pharmgkbrs1057520367
gwascentralrs1057520367
openSNPrs1057520367
23andMers1057520367
23andMe allrs1057520367
SNPshotrs1057520367
SNPdbers1057520367
MSV3drs1057520367
GWAS Ctlgrs1057520367
Max Magnitude0
ClinVar
Risk rs1057520367(T;T)
Alt rs1057520367(T;T)
Reference Rs1057520367(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SETX
CLNDBN not provided
Reversed 1
HGVS NC_000009.11:g.135224793G>A
CLNSRC
CLNACC RCV000440159.1,