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rs1057519213

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs1057519213(-;T)
Make rs1057519213(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome9
Position132275313
GeneSETX
is asnp
is mentioned by
dbSNPrs1057519213
dbSNP (old)rs1057519213
ClinGenrs1057519213
ebirs1057519213
HLIrs1057519213
Exacrs1057519213
Gnomadrs1057519213
Varsomers1057519213
LitVarrs1057519213
Maprs1057519213
PheGenIrs1057519213
Biobankrs1057519213
1000 genomesrs1057519213
hgdprs1057519213
ensemblrs1057519213
gopubmedrs1057519213
geneviewrs1057519213
scholarrs1057519213
googlers1057519213
pharmgkbrs1057519213
gwascentralrs1057519213
openSNPrs1057519213
23andMers1057519213
23andMe allrs1057519213
SNPshotrs1057519213
SNPdbers1057519213
MSV3drs1057519213
GWAS Ctlgrs1057519213
Max Magnitude0
ClinVar
Risk rs1057519213(T;T)
Alt rs1057519213(T;T)
Reference Rs1057519213(-;-)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SETX
CLNDBN not provided
Reversed 1
HGVS NC_000009.11:g.135150701dupA
CLNSRC
CLNACC RCV000415862.1,