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rs121909488

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121909488(G;T)
Make rs121909488(T;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position126690862
GeneLMX1B
is asnp
is mentioned by
dbSNPrs121909488
ebirs121909488
HLIrs121909488
Exacrs121909488
Varsomers121909488
Maprs121909488
PheGenIrs121909488
hapmaprs121909488
1000 genomesrs121909488
hgdprs121909488
ensemblrs121909488
gopubmedrs121909488
geneviewrs121909488
scholarrs121909488
googlers121909488
pharmgkbrs121909488
gwascentralrs121909488
openSNPrs121909488
23andMers121909488
23andMe allrs121909488
SNP Nexus

SNPshotrs121909488
SNPdbers121909488
MSV3drs121909488
GWAS Ctlgrs121909488
Max Magnitude0
OMIM602575
Desc
Variant0004
Relatedalso
ClinVar
Risk rs121909488(T;T)
Alt rs121909488(T;T)
Reference rs121909488(G;G)
Significance Pathogenic
Disease Nail-patella syndrome
Variation info
Gene LMX1B
CLNDBN Nail-patella syndrome
Reversed 0
HGVS NC_000009.11:g.129453141G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000007418.2,