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rs534723946

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs534723946(A;A)
Make rs534723946(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome9
Position132330094
GeneSETX
is asnp
is mentioned by
dbSNPrs534723946
ebirs534723946
HLIrs534723946
Exacrs534723946
Varsomers534723946
Maprs534723946
PheGenIrs534723946
hapmaprs534723946
1000 genomesrs534723946
hgdprs534723946
ensemblrs534723946
gopubmedrs534723946
geneviewrs534723946
scholarrs534723946
googlers534723946
pharmgkbrs534723946
gwascentralrs534723946
openSNPrs534723946
23andMers534723946
23andMe allrs534723946
SNP Nexus

SNPshotrs534723946
SNPdbers534723946
MSV3drs534723946
GWAS Ctlgrs534723946
Max Magnitude0
ClinVar
Risk rs534723946(A;A)
Alt rs534723946(A;A)
Reference rs534723946(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SETX
CLNDBN not provided
Reversed 0
HGVS NC_000009.11:g.135205481G>A
CLNSRC
CLNACC RCV000143813.1,