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rs121909489

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121909489(C;T)
Make rs121909489(T;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position126615487
GeneLMX1B
is asnp
is mentioned by
dbSNPrs121909489
ebirs121909489
HLIrs121909489
Exacrs121909489
Varsomers121909489
Maprs121909489
PheGenIrs121909489
hapmaprs121909489
1000 genomesrs121909489
hgdprs121909489
ensemblrs121909489
gopubmedrs121909489
geneviewrs121909489
scholarrs121909489
googlers121909489
pharmgkbrs121909489
gwascentralrs121909489
openSNPrs121909489
23andMers121909489
23andMe allrs121909489
SNP Nexus

SNPshotrs121909489
SNPdbers121909489
MSV3drs121909489
GWAS Ctlgrs121909489
Max Magnitude0
OMIM602575
Desc
Variant0006
Relatedalso
ClinVar
Risk rs121909489(T;T)
Alt rs121909489(T;T)
Reference rs121909489(C;C)
Significance Pathogenic
Disease Nail-patella syndrome
Variation info
Gene LMX1B
CLNDBN Nail-patella syndrome
Reversed 0
HGVS NC_000009.11:g.129377766C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000007420.2,