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: rs10488140
rs10488140
EGFR
1.000 0.040 7 55070695 intron variant C/T snv 0.26
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder 		0.700 1.000 1 2008 2008
dbSNP: rs17172438
rs17172438
EGFR
1.000 0.040 7 55083844 intron variant T/C snv 0.21
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder 		0.700 1.000 1 2008 2008
dbSNP: rs729969
rs729969
EGFR
1.000 0.040 7 55060514 intron variant A/G;T snv
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder 		0.700 1.000 1 2008 2008