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rs864621969

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs864621969(C;G)
Make rs864621969(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position126615549
GeneLMX1B, LOC105376277
is asnp
is mentioned by
dbSNPrs864621969
ebirs864621969
HLIrs864621969
Exacrs864621969
Varsomers864621969
Maprs864621969
PheGenIrs864621969
hapmaprs864621969
1000 genomesrs864621969
hgdprs864621969
ensemblrs864621969
gopubmedrs864621969
geneviewrs864621969
scholarrs864621969
googlers864621969
pharmgkbrs864621969
gwascentralrs864621969
openSNPrs864621969
23andMers864621969
23andMe allrs864621969
SNP Nexus

SNPshotrs864621969
SNPdbers864621969
MSV3drs864621969
GWAS Ctlgrs864621969
Max Magnitude0
ClinVar
Risk rs864621969(G;G)
Alt rs864621969(G;G)
Reference rs864621969(C;C)
Significance Pathogenic
Disease Nail-patella syndrome
Variation info
Gene LMX1B
CLNDBN Nail-patella syndrome
Reversed 0
HGVS NC_000009.11:g.129377828C>G
CLNSRC
CLNACC RCV000205274.1,