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: rs10947055
rs10947055
3 6 30125587 intergenic variant T/C snv 0.11 0.700 1.000 1 2011 2011
dbSNP: rs12757165
rs12757165
2 1 216543195 intron variant A/G snv 0.29 0.700 1.000 1 2011 2011
dbSNP: rs12907914
rs12907914
2 15 39023157 intron variant G/C snv 0.30 0.700 1.000 1 2011 2011
dbSNP: rs1320448
rs1320448
2 10 104086316 upstream gene variant A/G snv 0.92 0.700 1.000 1 2011 2011
dbSNP: rs1484170
rs1484170
2 10 80939735 downstream gene variant T/C snv 0.17 0.700 1.000 1 2011 2011
dbSNP: rs152528
rs152528
2 5 142638295 intron variant C/T snv 0.28 0.700 1.000 1 2011 2011
dbSNP: rs16830359
rs16830359
3 1.000 0.080 1 43130713 intergenic variant G/A;T snv 0.700 1.000 1 2011 2011
dbSNP: rs17636733
rs17636733
2 15 25667192 intergenic variant T/C snv 0.41 0.700 1.000 1 2011 2011
dbSNP: rs1916521
rs1916521
2 10 55657201 intergenic variant C/T snv 0.36 0.700 1.000 1 2011 2011
dbSNP: rs3729931
rs3729931
2 3 12585017 intron variant G/A snv 0.35 0.43 0.700 1.000 1 2011 2011
dbSNP: rs796051877
rs796051877
GAA
11 0.807 0.320 17 80110055 splice region variant G/A snv 4.0E-06 0.700 1.000 1 2015 2015