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rs121909487

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121909487(C;T)
Make rs121909487(T;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position126693243
GeneLMX1B
is asnp
is mentioned by
dbSNPrs121909487
ebirs121909487
HLIrs121909487
Exacrs121909487
Varsomers121909487
Maprs121909487
PheGenIrs121909487
hapmaprs121909487
1000 genomesrs121909487
hgdprs121909487
ensemblrs121909487
gopubmedrs121909487
geneviewrs121909487
scholarrs121909487
googlers121909487
pharmgkbrs121909487
gwascentralrs121909487
openSNPrs121909487
23andMers121909487
23andMe allrs121909487
SNP Nexus

SNPshotrs121909487
SNPdbers121909487
MSV3drs121909487
GWAS Ctlgrs121909487
Max Magnitude0
OMIM602575
Desc
Variant0002
Relatedalso
ClinVar
Risk rs121909487(T;T)
Alt rs121909487(T;T)
Reference rs121909487(C;C)
Significance Pathogenic
Disease Nail-patella syndrome
Variation info
Gene LMX1B
CLNDBN Nail-patella syndrome
Reversed 0
HGVS NC_000009.11:g.129455522C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000007416.2,