Source: ALL
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs112673195
rs112673195
LINC02422
1 12 31908519 intron variant G/A;C snv 0.700 1.000 1 2015 2015
dbSNP: rs150663673
rs150663673
LINC01516
1 10 25118280 intron variant G/A snv 1.3E-02 0.700 1.000 1 2015 2015
dbSNP: rs4767841
rs4767841
CIT
1 12 119724394 intron variant G/A snv 0.55 0.700 1.000 1 2015 2015
dbSNP: rs7124972
rs7124972 		1 11 81291756 intron variant C/T snv 7.7E-02 0.700 1.000 1 2015 2015
dbSNP: rs72881251
rs72881251
ZNF521
1 18 25094696 intron variant T/C snv 0.14 0.700 1.000 1 2015 2015
dbSNP: rs7704641
rs7704641
ADAMTS16 ; LOC101929200
1 5 5260570 intron variant G/A snv 0.37 0.700 1.000 1 2015 2015