Source: ALL
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: rs10084334
rs10084334
HEATR5B
1 2 37023748 intron variant C/G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs10177191
rs10177191
LOC105373414
1 2 9106592 upstream gene variant T/C snv 0.46 0.700 1.000 1 2019 2019
dbSNP: rs10188118
rs10188118 		1 2 653623 intergenic variant C/G snv 0.33 0.700 1.000 1 2019 2019
dbSNP: rs10198459
rs10198459 		1 2 176408544 intergenic variant T/A;C;G snv 0.700 1.000 1 2019 2019
dbSNP: rs10208940
rs10208940
APLF
1 2 68506257 intron variant T/C snv 0.23 0.700 1.000 1 2015 2015
dbSNP: rs1035941
rs1035941
INSR
1 19 7199928 intron variant A/G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs10405423
rs10405423
INSR
1 19 7211300 intron variant C/A;G snv 0.700 1.000 1 2019 2019
dbSNP: rs10414501
rs10414501
TSKS ; LOC105372434
1 19 49756417 intron variant C/G snv 5.8E-02 0.700 1.000 1 2019 2019
dbSNP: rs10418164
rs10418164
CEP89
1 19 32920233 intron variant T/G snv 0.64 0.700 1.000 1 2019 2019
dbSNP: rs10423138
rs10423138
ZNF584
1 19 58416935 synonymous variant T/A;C snv 0.45 0.700 1.000 1 2017 2017
dbSNP: rs10438961
rs10438961 		1 18 45199142 intergenic variant T/G snv 0.25 0.700 1.000 1 2019 2019
dbSNP: rs10769187
rs10769187
LOC105376661
1 11 46125304 intron variant A/G snv 0.34 0.700 1.000 1 2019 2019
dbSNP: rs10803394
rs10803394
DNAJC16 ; AGMAT
1 1 15582985 intron variant G/A;C snv 0.700 1.000 1 2019 2019
dbSNP: rs10886117
rs10886117
LOC107984274
1 10 117721067 TF binding site variant G/A snv 0.14 0.700 1.000 1 2019 2019
dbSNP: rs10890263
rs10890263
PTPRF
1 1 43595361 intron variant T/C snv 0.20 0.700 1.000 1 2019 2019
dbSNP: rs10892354
rs10892354
USP2 ; USP2-AS1
1 11 119367671 intron variant T/A;C;G snv 0.700 1.000 1 2019 2019
dbSNP: rs10896028
rs10896028
RELA ; RELA-DT
1 11 65664716 non coding transcript exon variant A/T snv 0.36 0.700 1.000 1 2019 2019
dbSNP: rs10901057
rs10901057 		1 9 131370311 upstream gene variant C/A;G snv 0.700 1.000 1 2019 2019
dbSNP: rs10908521
rs10908521
INSRR ; NTRK1
1 1 156843858 intron variant T/C snv 0.31 0.700 1.000 1 2017 2017
dbSNP: rs10942549
rs10942549
TMEM171
1 5 73130310 intron variant G/C;T snv 0.700 1.000 1 2019 2019
dbSNP: rs10956924
rs10956924
ESRP1
1 8 94666084 intron variant T/C snv 0.69 0.700 1.000 1 2019 2019
dbSNP: rs10971419
rs10971419
B4GALT1
1 9 33124163 intron variant T/C snv 0.37 0.700 1.000 1 2019 2019
dbSNP: rs10971420
rs10971420
B4GALT1
1 9 33125002 intron variant T/C snv 0.37 0.700 1.000 1 2019 2019
dbSNP: rs11066390
rs11066390
RPH3A
1 12 112725961 intron variant A/G snv 0.76 0.700 1.000 1 2019 2019
dbSNP: rs11070231
rs11070231
FSIP1
1 15 39729375 intron variant A/C snv 0.44 0.700 1.000 1 2019 2019