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: rs10065321
rs10065321
1 5 142477850 intron variant C/T snv 0.38 0.700 1.000 1 2019 2019
dbSNP: rs1006705
rs1006705
1 12 54065146 intron variant A/G snv 0.66 0.700 1.000 1 2019 2019
dbSNP: rs1007330
rs1007330
1 20 46897482 intron variant C/T snv 0.33 0.700 1.000 1 2019 2019
dbSNP: rs10083447
rs10083447
1 14 91998083 intron variant G/A snv 0.52 0.700 1.000 1 2019 2019
dbSNP: rs10101067
rs10101067
2 8 71495139 intron variant G/C snv 6.2E-02 0.700 1.000 1 2019 2019
dbSNP: rs10116353
rs10116353
1 9 109187808 intron variant G/T snv 0.32 0.700 1.000 1 2019 2019
dbSNP: rs10125521
rs10125521
1 9 106300721 intron variant G/A;C;T snv 0.700 1.000 1 2019 2019
dbSNP: rs10152595
rs10152595
2 1.000 0.080 15 67183150 intron variant C/G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs10164099
rs10164099
1 18 37110781 intron variant T/C snv 0.15 0.700 1.000 1 2019 2019
dbSNP: rs1017698
rs1017698
1 2 218305802 intron variant G/A;C snv 0.700 1.000 1 2019 2019
dbSNP: rs10177093
rs10177093
1 2 187349092 intron variant G/T snv 0.55 0.700 1.000 1 2019 2019
dbSNP: rs10190249
rs10190249
1 2 66015391 intron variant G/A snv 0.24 0.700 1.000 1 2019 2019
dbSNP: rs1020731
rs1020731
2 1.000 0.080 2 160287544 intron variant G/A snv 0.69 0.700 1.000 1 2019 2019
dbSNP: rs10264590
rs10264590
1 7 77728431 intron variant A/G snv 0.58 0.700 1.000 1 2018 2018
dbSNP: rs10270542
rs10270542
2 7 77894452 intron variant A/G snv 0.43 0.700 1.000 1 2019 2019
dbSNP: rs1034207
rs1034207
1 6 127016554 intron variant C/A;G;T snv 0.94 0.700 1.000 1 2010 2010
dbSNP: rs1035940
rs1035940
1 19 7199967 intron variant C/A;G snv 0.700 1.000 1 2019 2019
dbSNP: rs10460716
rs10460716
1 21 38084132 intron variant T/A snv 0.53 0.700 1.000 1 2019 2019
dbSNP: rs10499013
rs10499013
1 6 97498520 intron variant G/A;T snv 0.700 1.000 1 2019 2019
dbSNP: rs10502148
rs10502148
1 11 111777274 intron variant C/T snv 0.33 0.700 1.000 1 2018 2018
dbSNP: rs10512606
rs10512606
1 17 76215127 intron variant A/C snv 0.14 0.700 1.000 1 2018 2018
dbSNP: rs10743098
rs10743098
1 11 9038003 intron variant A/G snv 0.42 0.700 1.000 1 2019 2019
dbSNP: rs10761785
rs10761785
3 10 63559006 intron variant G/T snv 0.51 0.700 1.000 1 2019 2019
dbSNP: rs10808546
rs10808546
7 8 125483576 intron variant C/T snv 0.39 0.700 1.000 1 2019 2019
dbSNP: rs10820747
rs10820747
1 9 104924542 intron variant G/A snv 0.27 0.700 1.000 1 2019 2019