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rs1057520783

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057520783(G;G)
Make rs1057520783(G;T)
ReferenceGRCh38.p7 38.3/150
Chromosome9
Position126615469
GeneLMX1B, LOC105376277
is asnp
is mentioned by
dbSNPrs1057520783
dbSNP (old)rs1057520783
ClinGenrs1057520783
ebirs1057520783
HLIrs1057520783
Exacrs1057520783
Gnomadrs1057520783
Varsomers1057520783
LitVarrs1057520783
Maprs1057520783
PheGenIrs1057520783
Biobankrs1057520783
1000 genomesrs1057520783
hgdprs1057520783
ensemblrs1057520783
gopubmedrs1057520783
geneviewrs1057520783
scholarrs1057520783
googlers1057520783
pharmgkbrs1057520783
gwascentralrs1057520783
openSNPrs1057520783
23andMers1057520783
23andMe allrs1057520783
SNPshotrs1057520783
SNPdbers1057520783
MSV3drs1057520783
GWAS Ctlgrs1057520783
Max Magnitude0
ClinVar
Risk rs1057520783(G;G)
Alt rs1057520783(G;G)
Reference Rs1057520783(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene LMX1B
CLNDBN not provided
Reversed 0
HGVS NC_000009.11:g.129377748T>G
CLNSRC
CLNACC RCV000421725.1,