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rs121909490

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121909490(C;T)
Make rs121909490(T;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position126693273
GeneLMX1B
is asnp
is mentioned by
dbSNPrs121909490
ebirs121909490
HLIrs121909490
Exacrs121909490
Varsomers121909490
Maprs121909490
PheGenIrs121909490
hapmaprs121909490
1000 genomesrs121909490
hgdprs121909490
ensemblrs121909490
gopubmedrs121909490
geneviewrs121909490
scholarrs121909490
googlers121909490
pharmgkbrs121909490
gwascentralrs121909490
openSNPrs121909490
23andMers121909490
23andMe allrs121909490
SNP Nexus

SNPshotrs121909490
SNPdbers121909490
MSV3drs121909490
GWAS Ctlgrs121909490
Max Magnitude0
OMIM602575
Desc
Variant0007
Relatedalso
ClinVar
Risk rs121909490(T;T)
Alt rs121909490(T;T)
Reference Rs121909490(C;C)
Significance Pathogenic
Disease Nail-patella syndrome
Variation info
Gene LMX1B
CLNDBN Nail-patella syndrome
Reversed 0
HGVS NC_000009.11:g.129455552C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000007421.2,