Source: ALL

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: rs11206019
rs11206019
1 52794278 intron variant G/T snv 0.16
CUI: C1704436
Disease: Peripheral Arterial Diseases
Peripheral Arterial Diseases
0.700 1.000 1 2016 2016
dbSNP: rs505444
rs505444
1.000 0.080 1 52786188 intron variant T/A;C;G snv
CUI: C0027404
Disease: Narcolepsy
Narcolepsy
0.700 1.000 1 2009 2009