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: rs6479874
rs6479874
PRKG1
10 51029595 intron variant T/C snv 0.88
CUI: C0149931
Disease: Migraine Disorders
Migraine Disorders 		0.800 1.000 1 2013 2013
dbSNP: rs7922491
rs7922491
PRKG1
1.000 0.080 10 51733713 intron variant G/A;T snv
CUI: C0004096
Disease: Asthma
Asthma 		0.800 1.000 1 2011 2011
dbSNP: rs10762524
rs10762524
PRKG1
1.000 0.040 10 52014152 intron variant T/A;C;G snv
CUI: C1263846
Disease: Attention deficit hyperactivity disorder
Attention deficit hyperactivity disorder 		0.700 1.000 1 2010 2010
dbSNP: rs10823964
rs10823964
PRKG1
1.000 0.040 10 52017283 intron variant T/G snv 0.51
CUI: C1263846
Disease: Attention deficit hyperactivity disorder
Attention deficit hyperactivity disorder 		0.700 1.000 1 2010 2010
dbSNP: rs10823973
rs10823973
PRKG1
1.000 0.040 10 52019720 intron variant C/G;T snv
CUI: C1263846
Disease: Attention deficit hyperactivity disorder
Attention deficit hyperactivity disorder 		0.700 1.000 1 2010 2010