Have questions? Visit https://www.reddit.com/r/SNPedia

rs121909492

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121909492(C;T)
Make rs121909492(T;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position126693527
GeneLMX1B
is asnp
is mentioned by
dbSNPrs121909492
ebirs121909492
HLIrs121909492
Exacrs121909492
Varsomers121909492
Maprs121909492
PheGenIrs121909492
hapmaprs121909492
1000 genomesrs121909492
hgdprs121909492
ensemblrs121909492
gopubmedrs121909492
geneviewrs121909492
scholarrs121909492
googlers121909492
pharmgkbrs121909492
gwascentralrs121909492
openSNPrs121909492
23andMers121909492
23andMe allrs121909492
SNP Nexus

SNPshotrs121909492
SNPdbers121909492
MSV3drs121909492
GWAS Ctlgrs121909492
Max Magnitude0
OMIM602575
Desc
Variant0011
Relatedalso
ClinVar
Risk rs121909492(T;T)
Alt rs121909492(T;T)
Reference rs121909492(C;C)
Significance Pathogenic
Disease Nail-patella syndrome
Variation info
Gene LMX1B
CLNDBN Nail-patella syndrome
Reversed 0
HGVS NC_000009.11:g.129455806C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000007425.2,