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rs1057520178

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(CTTCC;CTTCC) 0 common in clinvar
Make rs1057520178(-;-)
Make rs1057520178(-;CTTCC)
ReferenceGRCh38.p7 38.3/150
Chromosome9
Position126615528
GeneLMX1B, LOC105376277
is asnp
is mentioned by
dbSNPrs1057520178
dbSNP (old)rs1057520178
ClinGenrs1057520178
ebirs1057520178
HLIrs1057520178
Exacrs1057520178
Gnomadrs1057520178
Varsomers1057520178
Maprs1057520178
PheGenIrs1057520178
Biobankrs1057520178
1000 genomesrs1057520178
hgdprs1057520178
ensemblrs1057520178
gopubmedrs1057520178
geneviewrs1057520178
scholarrs1057520178
googlers1057520178
pharmgkbrs1057520178
gwascentralrs1057520178
openSNPrs1057520178
23andMers1057520178
23andMe allrs1057520178
SNPshotrs1057520178
SNPdbers1057520178
MSV3drs1057520178
GWAS Ctlgrs1057520178
Max Magnitude0
ClinVar
Risk rs1057520178(-;-)
Alt rs1057520178(-;-)
Reference Rs1057520178(CTTCC;CTTCC)
Significance Pathogenic
Disease not provided
Variation info
Gene LMX1B
CLNDBN not provided
Reversed 0
HGVS NC_000009.11:g.129377807_129377811delCTTCC
CLNSRC
CLNACC RCV000424540.1,