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rs121909491

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121909491(A;A)
Make rs121909491(A;G)
ReferenceGRCh38 38.1/141
Chromosome9
Position126693250
GeneLMX1B
is asnp
is mentioned by
dbSNPrs121909491
ebirs121909491
HLIrs121909491
Exacrs121909491
Varsomers121909491
Maprs121909491
PheGenIrs121909491
hapmaprs121909491
1000 genomesrs121909491
hgdprs121909491
ensemblrs121909491
gopubmedrs121909491
geneviewrs121909491
scholarrs121909491
googlers121909491
pharmgkbrs121909491
gwascentralrs121909491
openSNPrs121909491
23andMers121909491
23andMe allrs121909491
SNP Nexus

SNPshotrs121909491
SNPdbers121909491
MSV3drs121909491
GWAS Ctlgrs121909491
Merged fromRs28939692
Max Magnitude0
OMIM602575
Desc
Variant0008
Relatedalso
ClinVar
Risk rs121909491(A;A)
Alt rs121909491(A;A)
Reference rs121909491(G;G)
Significance Pathogenic
Disease Nail-patella syndrome
Variation info
Gene LMX1B
CLNDBN Nail-patella syndrome
Reversed 0
HGVS NC_000009.11:g.129455529G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000007422.2,