{{Rsnum
|rsid = 12937241
|geno1 = (A;A)
|geno2 = (A;T)
|geno3 = (T;T)
|Status = Merged
|Merged = 1126821
|Gene = JUP
|Orientation=minus
|ReferenceAllele=A
|MissenseAllele=T
|Chromosome=17
|position=41755893
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=JUP
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;T)
| geno3=(T;T)
| CEU | 6.3 | 42.9 | 50.8
| HCB | 47.7 | 45.5 | 6.8
| JPT | 25.6 | 55.8 | 18.6
| YRI | 31.1 | 37.7 | 31.1
| ASW | 0.0 | 0.0 | 0.0
| CHB | 47.7 | 45.5 | 6.8
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 0.0 | 0.0 | 0.0
| MEX | 0.0 | 0.0 | 0.0
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=28
}}

{{Venter SNP
|rsid=12937241
|allele=A
|frequency=
|uid=1103645325133
|type=homozygous_SNP
|hugo=JUP
|ensembl gene=ENSG00000173801
|ensembl transcript=ENST00000310706
|sift=TOLERATED
|disease=Defects in JUP are the cause of Naxos disease (MIM:601214). Naxos disease is an autosomal recessive disorder combining non-epidermolytic palmoplantar keratoderma with arrhythmogenic right ventricular cardiomyopathy and wooly hair.
}}