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: rs2255141
rs2255141
5 10 112174128 intron variant A/G;T snv 0.800 1.000 3 2010 2018
dbSNP: rs1129555
rs1129555
5 10 112150963 3 prime UTR variant A/G snv 0.71 0.700 1.000 3 2015 2018
dbSNP: rs7096937
rs7096937
5 10 112190660 intron variant T/C snv 0.72 0.700 1.000 2 2018 2019
dbSNP: rs2297991
rs2297991
4 10 112153464 3 prime UTR variant T/C snv 0.69 0.700 1.000 1 2018 2018
dbSNP: rs2803621
rs2803621
4 10 112179826 intron variant G/A snv 0.74 0.700 1.000 1 2018 2018
dbSNP: rs77147124
rs77147124
4 10 112159366 intron variant A/G snv 0.700 1.000 1 2018 2018
dbSNP: rs77987196
rs77987196
2 10 112173249 intron variant TT/-;T;TTT delins 0.71 0.700 1.000 1 2018 2018