Source: GWASCAT ×
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: rs1415701
rs1415701
2 6 130024690 intron variant G/A snv 0.31 0.700 1.000 3 2013 2019
dbSNP: rs6569648
rs6569648
5 1.000 0.080 6 130027974 intron variant C/T snv 0.84 0.700 1.000 2 2010 2019
dbSNP: rs7740107
rs7740107
6 1.000 0.080 6 130053316 intron variant T/A;G snv 0.700 1.000 2 2014 2019
dbSNP: rs113898003
rs113898003
1 6 130020090 intron variant T/C snv 0.32 0.700 1.000 1 2017 2017
dbSNP: rs12661188
rs12661188
2 6 130057688 intron variant T/A;C snv 0.700 1.000 1 2017 2017
dbSNP: rs17633311
rs17633311
1 6 130127708 intron variant C/T snv 2.4E-02 0.700 1.000 1 2019 2019
dbSNP: rs6569647
rs6569647
2 6 130016121 intron variant T/C snv 0.34 0.700 1.000 1 2019 2019