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: rs1002054
rs1002054
1 14 55062195 intron variant A/C;T snv 0.700 1.000 1 2012 2012
dbSNP: rs17128143
rs17128143
1 14 55066870 3 prime UTR variant C/G snv 7.4E-02 0.700 1.000 1 2012 2012
dbSNP: rs2251366
rs2251366
1 14 55051438 upstream gene variant A/G snv 0.52 0.700 1.000 1 2012 2012
dbSNP: rs2340943
rs2340943
1 14 55051289 upstream gene variant C/T snv 0.27 0.700 1.000 1 2012 2012
dbSNP: rs3742564
rs3742564
1 14 55063402 intron variant T/C snv 0.49 0.700 1.000 1 2012 2012