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rs10733682

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs10733682(A;G)
Make rs10733682(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome9
Position126698635
GeneLMX1B
is asnp
is mentioned by
dbSNPrs10733682
dbSNP (old)rs10733682
ClinGenrs10733682
ebirs10733682
HLIrs10733682
Exacrs10733682
Gnomadrs10733682
Varsomers10733682
Maprs10733682
PheGenIrs10733682
Biobankrs10733682
1000 genomesrs10733682
hgdprs10733682
ensemblrs10733682
gopubmedrs10733682
geneviewrs10733682
scholarrs10733682
googlers10733682
pharmgkbrs10733682
gwascentralrs10733682
openSNPrs10733682
23andMers10733682
23andMe allrs10733682
SNPshotrs10733682
SNPdbers10733682
MSV3drs10733682
GWAS Ctlgrs10733682
Max Magnitude0
? (A;A) (A;G) (G;G) 28
[PMID 28245097] Influence of genetic variants associated with body mass index on eating behavior in childhood.


ClinVar
Risk rs10733682(G;G)
Alt rs10733682(G;G)
Reference Rs10733682(A;A)
Significance Non-pathogenic
Disease Nail-patella syndrome
Variation info
Gene LMX1B
CLNDBN Nail-patella syndrome
Reversed 0
HGVS NC_000009.11:g.129460914A>G
CLNSRC
CLNACC RCV000360275.1,