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rs1057522039

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057522039(C;T)
Make rs1057522039(T;T)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position65514854
GeneLAS1L
is asnp
is mentioned by
dbSNPrs1057522039
dbSNP (old)rs1057522039
ClinGenrs1057522039
ebirs1057522039
HLIrs1057522039
Exacrs1057522039
Gnomadrs1057522039
Varsomers1057522039
LitVarrs1057522039
Maprs1057522039
PheGenIrs1057522039
Biobankrs1057522039
1000 genomesrs1057522039
hgdprs1057522039
ensemblrs1057522039
gopubmedrs1057522039
geneviewrs1057522039
scholarrs1057522039
googlers1057522039
pharmgkbrs1057522039
gwascentralrs1057522039
openSNPrs1057522039
23andMers1057522039
23andMe allrs1057522039
SNPshotrs1057522039
SNPdbers1057522039
MSV3drs1057522039
GWAS Ctlgrs1057522039
Max Magnitude0
ClinVar
Risk rs1057522039(T;T)
Alt rs1057522039(T;T)
Reference Rs1057522039(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene LAS1L
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.64734734G>A
CLNSRC
CLNACC RCV000418984.1,