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rs28939692

From SNPedia

Merged intors121909491
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0
Make rs28939692(A;A)
Make rs28939692(A;G)
ReferenceGRCh38 38.1/141
Chromosome9
Position126693250
GeneLMX1B
is asnp
is mentioned by
dbSNPrs28939692
dbSNP (old)rs28939692
ClinGenrs28939692
ebirs28939692
HLIrs28939692
Exacrs28939692
Gnomadrs28939692
Varsomers28939692
Maprs28939692
PheGenIrs28939692
Biobankrs28939692
1000 genomesrs28939692
hgdprs28939692
ensemblrs28939692
gopubmedrs28939692
geneviewrs28939692
scholarrs28939692
googlers28939692
pharmgkbrs28939692
gwascentralrs28939692
openSNPrs28939692
23andMers28939692
23andMe allrs28939692
SNP Nexus

SNPshotrs28939692
SNPdbers28939692
MSV3drs28939692
GWAS Ctlgrs28939692
StatusMerged into rs121909491
Max Magnitude0
OMIM602575
DescNAIL-PATELLA SYNDROME
Variant0008
Relatedalso