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: rs12104221
rs12104221
19 3797102 intron variant C/T snv 0.14
CUI: C0162701
Disease: Polysomnography
Polysomnography
0.700 1.000 1 2012 2012