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rs1057516196

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs1057516196(-;C)
Make rs1057516196(C;C)
ReferenceGRCh38.p7 38.3/150
Chromosome9
Position126615435
GeneLMX1B, LOC105376277
is asnp
is mentioned by
dbSNPrs1057516196
dbSNP (old)rs1057516196
ClinGenrs1057516196
ebirs1057516196
HLIrs1057516196
Exacrs1057516196
Gnomadrs1057516196
Varsomers1057516196
Maprs1057516196
PheGenIrs1057516196
Biobankrs1057516196
1000 genomesrs1057516196
hgdprs1057516196
ensemblrs1057516196
gopubmedrs1057516196
geneviewrs1057516196
scholarrs1057516196
googlers1057516196
pharmgkbrs1057516196
gwascentralrs1057516196
openSNPrs1057516196
23andMers1057516196
23andMe allrs1057516196
SNPshotrs1057516196
SNPdbers1057516196
MSV3drs1057516196
GWAS Ctlgrs1057516196
Max Magnitude0
ClinVar
Risk rs1057516196(C;C)
Alt rs1057516196(C;C)
Reference Rs1057516196(-;-)
Significance Probable-Pathogenic
Disease Nail-patella syndrome
Variation info
Gene LMX1B
CLNDBN Nail-patella syndrome
Reversed 0
HGVS NC_000009.11:g.129377714dupC
CLNSRC
CLNACC RCV000408886.1,