Source: GWASCAT

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: rs12185644
rs12185644 		1.000 2 57824634 intergenic variant C/A snv 0.66
CUI: C1838604
Disease: EPILEPSY, CHILDHOOD ABSENCE, 1
EPILEPSY, CHILDHOOD ABSENCE, 1 		0.700 1.000 1 2018 2018
dbSNP: rs13020210
rs13020210 		1.000 2 144623658 intergenic variant G/A snv 0.73
CUI: C1838604
Disease: EPILEPSY, CHILDHOOD ABSENCE, 1
EPILEPSY, CHILDHOOD ABSENCE, 1 		0.700 1.000 1 2018 2018