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: rs4871750
rs4871750
PCAT1 ; LOC105375751
8 126889758 intron variant G/A;C snv
CUI: C0162701
Disease: Polysomnography
Polysomnography 		0.700 1.000 1 2012 2012
dbSNP: rs4871752
rs4871752
PCAT1 ; LOC105375751
8 126908341 intron variant G/A snv 0.43
CUI: C0162701
Disease: Polysomnography
Polysomnography 		0.700 1.000 1 2012 2012
dbSNP: rs7012789
rs7012789
PCAT1 ; LOC105375751
8 126904963 intron variant A/G;T snv
CUI: C0162701
Disease: Polysomnography
Polysomnography 		0.700 1.000 1 2012 2012
dbSNP: rs7817717
rs7817717
PCAT1 ; LOC105375751
8 126891017 intron variant T/G snv 0.43
CUI: C0162701
Disease: Polysomnography
Polysomnography 		0.700 1.000 1 2012 2012