JCAD

junctional cadherin 5 associated

Summary

This gene encodes an endothelial cell-to-cell junction protein. Naturally occurring mutations in this gene are associated with coronary artery disease, late onset alzheimer disease, and emphysema distribution. [provided by RefSeq, Mar 2017]

Known Variants112 total

rsidPosition (GRCh37)AllelesClassClinVar
rs1181460310:30,308,303A/Gintron variant—
rs120258985910:30,315,048T/G—uncertain significance
rs90392438410:30,315,098T/C—uncertain significance
rs7662261310:30,315,181G/A—benign
rs74764557310:30,315,191C/A—uncertain significance
rs11702973410:30,315,222G/A—benign
rs6174102610:30,315,239C/T—benign
rs37337660910:30,315,268C/T—uncertain significance
rs77733729510:30,315,269G/A—uncertain significance
rs37661363310:30,315,304C/T—uncertain significance
rs20053634910:30,315,319C/T—uncertain significance
rs7460126810:30,315,328G/A—uncertain significance
rs20023716410:30,315,358A/G—uncertain significance
rs37381581210:30,315,385T/C—uncertain significance
rs20151499610:30,315,394C/T—uncertain significance
rs74696903010:30,315,407G/A—uncertain significance
rs249161747810:30,315,413T/C—uncertain significance
rs36849705710:30,315,473C/T—uncertain significance
rs77114966910:30,315,572C/G—uncertain significance
rs37515020710:30,315,574C/T—uncertain significance
rs36813942010:30,315,575G/C—uncertain significance
rs249161809010:30,315,614T/C—likely benign
rs52769822610:30,315,623C/T—uncertain significance
rs75480930710:30,315,627C/A—uncertain significance
rs249161819510:30,315,650C/G—uncertain significance
rs131707410710:30,315,655G/C—uncertain significance
rs183681525010:30,315,664G/C—uncertain significance
rs37275479710:30,315,685C/T—uncertain significance
rs75513026210:30,315,941G/C—uncertain significance
rs183683125810:30,315,979G/A—uncertain significance
rs37504984010:30,315,993C/G—uncertain significance
rs148459062810:30,315,994C/G—uncertain significance
rs156444203910:30,316,019G/A—uncertain significance
rs88841656810:30,316,025C/G—uncertain significance
rs373999810:30,316,072C/Amissense variant—
rs14280600810:30,316,075T/C—uncertain significance
rs19006789910:30,316,081G/A—uncertain significance
rs37559460710:30,316,124C/A—uncertain significance
rs75406486610:30,316,253C/T—uncertain significance
rs19997647210:30,316,377C/A—uncertain significance
rs100701510810:30,316,396G/C—uncertain significance
rs142868306110:30,316,424T/C—uncertain significance
rs74699203410:30,316,474T/C—uncertain significance
rs74825740510:30,316,480G/A—uncertain significance
rs156444291610:30,316,507C/T—uncertain significance
rs77592932510:30,316,543T/C—uncertain significance
rs156444314210:30,316,667C/T—uncertain significance
rs37510440110:30,316,681C/T—uncertain significance
rs90985057010:30,316,682G/A—uncertain significance
rs20191552410:30,316,789G/A—uncertain significance
rs36836746610:30,316,795T/C—uncertain significance
rs77062072010:30,316,869G/C—likely benign
rs116166475410:30,316,923C/A—uncertain significance
rs249162355810:30,316,933C/G—uncertain significance
rs74539740710:30,316,972G/C—uncertain significance
rs18712191710:30,317,039A/G—uncertain significance
rs57256345110:30,317,063G/A—uncertain significance
rs20122072410:30,317,128T/G—uncertain significance
rs19245888510:30,317,230C/A—uncertain significance
rs20044467410:30,317,251T/C—uncertain significance
rs19984939510:30,317,276T/G—uncertain significance
rs149040156510:30,317,323A/C—uncertain significance
rs37766556710:30,317,420C/T—uncertain significance
rs75027657710:30,317,474C/T—uncertain significance
rs37561170510:30,317,498G/T—uncertain significance
rs93889421910:30,317,519A/G—uncertain significance
rs57189095110:30,317,522G/A—uncertain significance
rs76002633910:30,317,557T/C—uncertain significance
rs53900249210:30,317,561C/T—likely benign
rs15097414810:30,317,584C/G—uncertain significance
rs791756610:30,317,597C/G—uncertain significance
rs95535295210:30,317,612C/T—uncertain significance
rs76736741410:30,317,632G/T—uncertain significance
rs75744043010:30,317,652C/A—uncertain significance
rs124699413610:30,317,684G/A—uncertain significance
rs77242703710:30,317,687C/T—uncertain significance
rs37200418410:30,317,698G/A—uncertain significance
rs77408841910:30,317,719T/C—uncertain significance
rs76546247610:30,317,744C/T—uncertain significance
rs19011615210:30,317,782C/T—uncertain significance
rs37249316110:30,317,852C/T—uncertain significance
rs20096928010:30,317,980A/T—uncertain significance
rs75799670410:30,317,995G/C—uncertain significance
rs75442309410:30,318,116C/T—likely benign
rs183692675710:30,318,126C/A—uncertain significance
rs77221295610:30,318,167A/G—uncertain significance
rs249162851710:30,318,194G/A—uncertain significance
rs37153029310:30,318,231G/A—likely benign
rs19985877110:30,318,281C/T—likely benign
rs97436838410:30,318,283C/G—uncertain significance
rs141400973310:30,318,325T/C—likely benign
rs75079834310:30,318,362C/T—uncertain significance
rs117323724010:30,318,403T/C—likely benign
rs77620882810:30,318,419C/T—uncertain significance
rs77292941810:30,318,556C/T—uncertain significance
rs4128475210:30,318,705C/T—likely benign
rs37702466010:30,318,715T/C—uncertain significance
rs75082580210:30,318,718C/T—uncertain significance
rs20009425410:30,318,719G/A—uncertain significance
rs75863583510:30,318,730C/T—uncertain significance

Showing 100 of 112 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.