Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs4282438
rs4282438
0.807 0.280 6 33104395 intron variant T/G snv 3.1E-02
CUI: C1527336
Disease: Sjogren's Syndrome
Sjogren's Syndrome
0.800 1.000 1 2013 2013
dbSNP: rs4282438
rs4282438
0.807 0.280 6 33104395 intron variant T/G snv 3.1E-02
CUI: C4048328
Disease: cervical cancer
cervical cancer
0.730 1.000 1 2013 2016