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: rs111033220
rs111033220
4 0.925 0.160 7 107690203 missense variant C/G;T snv 4.0E-06; 1.8E-04 0.800 1.000 33 1998 2019
dbSNP: rs111033305
rs111033305
4 0.925 0.160 7 107690200 missense variant G/A;C snv 1.0E-04; 8.0E-06 0.800 1.000 25 1998 2019
dbSNP: rs28939086
rs28939086
4 0.925 0.160 7 107690220 missense variant A/C;G snv 2.0E-04; 4.0E-06 0.800 1.000 24 1998 2019
dbSNP: rs111033307
rs111033307
6 0.851 0.240 7 107694473 missense variant T/G snv 1.0E-04 7.7E-05 0.800 1.000 22 1998 2018
dbSNP: rs111033308
rs111033308
2 0.925 0.160 7 107695984 missense variant G/A;C snv 2.0E-05 6.3E-05 0.800 1.000 19 1998 2018
dbSNP: rs201562855
rs201562855
4 0.925 0.160 7 107690148 missense variant A/T snv 4.0E-06 0.800 1.000 19 1998 2019
dbSNP: rs111033256
rs111033256
3 0.882 0.160 7 107675060 missense variant T/A snv 2.0E-04 3.5E-05 0.800 1.000 17 1998 2019
dbSNP: rs121908363
rs121908363
4 0.925 0.160 7 107710126 missense variant C/T snv 5.2E-05 2.8E-05 0.800 1.000 17 1998 2017
dbSNP: rs121908361
rs121908361
3 0.882 0.160 7 107689156 stop gained A/G;T snv 0.800 1.000 16 1998 2017
dbSNP: rs121908364
rs121908364
3 0.925 0.160 7 107689166 missense variant C/T snv 0.800 1.000 16 1998 2017
dbSNP: rs763006761
rs763006761
3 0.925 0.160 7 107700135 missense variant A/G snv 1.6E-05 0.800 1.000 14 1998 2017
dbSNP: rs121908362
rs121908362
5 0.882 0.280 7 107710132 missense variant A/G snv 1.2E-04 3.5E-05 0.800 1.000 13 1998 2017
dbSNP: rs1554359670
rs1554359670
2 0.925 0.160 7 107694650 missense variant C/A snv 0.800 1.000 13 1998 2017
dbSNP: rs370588279
rs370588279
2 0.925 0.160 7 107663400 stop gained C/A;T snv 4.0E-06; 2.0E-05 0.800 1.000 13 1998 2017
dbSNP: rs111033212
rs111033212
4 0.851 0.240 7 107689054 missense variant T/A;C snv 4.0E-06; 8.6E-04 0.800 1.000 12 1998 2017
dbSNP: rs111033303
rs111033303
2 0.925 0.160 7 107674970 missense variant G/T snv 3.0E-04 3.8E-04 0.800 1.000 12 1998 2017
dbSNP: rs111033318
rs111033318
3 0.925 0.160 7 107702050 missense variant T/A snv 0.800 1.000 12 1998 2017
dbSNP: rs145254330
rs145254330
2 0.925 0.160 7 107672182 missense variant C/T snv 3.3E-04 1.7E-04 0.800 1.000 12 1998 2017
dbSNP: rs80338848
rs80338848
6 0.851 0.240 7 107675051 missense variant T/C snv 2.7E-04 3.4E-04 0.800 1.000 12 1998 2017
dbSNP: rs1554354370
rs1554354370
1 1.000 0.120 7 107672228 missense variant C/T snv 0.700 1.000 12 1998 2017
dbSNP: rs397516414
rs397516414
2 0.925 0.160 7 107690178 missense variant G/A snv 0.700 1.000 12 1998 2017
dbSNP: rs539699299
rs539699299
4 0.851 0.160 7 107661725 missense variant C/A;G snv 0.700 1.000 12 1998 2017
dbSNP: rs542620119
rs542620119
2 0.925 0.160 7 107674302 missense variant G/C snv 9.1E-05 3.5E-05 0.700 1.000 12 1998 2017
dbSNP: rs760413427
rs760413427
2 0.925 0.160 7 107674187 missense variant A/G snv 8.0E-06 0.700 1.000 12 1998 2017
dbSNP: rs192366176
rs192366176
4 0.925 0.160 7 107700180 splice region variant G/A snv 8.0E-06 1.4E-05 0.700 1.000 7 2005 2016