{{Rsnum
|rsid=34728766
|Gene=JAG2
|Chromosome=14
|position=105143063
|Orientation=plus
|ReferenceAllele=C
|MissenseAllele=T
|GMAF=0.005051
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=JAG2
}}{{Venter SNP
|rsid=34728766
|allele=A
|frequency=
|uid=1103649153732
|type=heterozygous_SNP
|hugo=JAG2
|ensembl gene=ENSG00000184916
|ensembl transcript=ENST00000331782
|sift=TOLERATED
|disease=May be associated with Usher syndrome type IA (USHA1A) which describes a congenital sensory deafness associated with retinitis pigmentosa and feeble-mindedness.
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | HumanOmni1Quad}}