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: rs374270497
rs374270497
ENPP1
2 0.925 0.040 6 131860504 missense variant C/A;T snv 2.0E-05 0.800 1.000 8 2003 2016
dbSNP: rs121918024
rs121918024
ENPP1
1 1.000 0.040 6 131877005 missense variant G/C snv 8.0E-06 7.0E-06 0.800 1.000 7 2003 2016
dbSNP: rs121918025
rs121918025
ENPP1
2 0.925 0.080 6 131861704 missense variant G/T snv 0.800 1.000 7 2003 2016
dbSNP: rs121918026
rs121918026
ENPP1
1 1.000 0.040 6 131864886 missense variant A/T snv 0.800 1.000 7 2003 2016
dbSNP: rs373044722
rs373044722
ENPP1
2 0.925 0.200 6 131872926 missense variant C/T snv 8.0E-06 0.800 1.000 7 2003 2016
dbSNP: rs387906673
rs387906673
ENPP1
1 1.000 0.040 6 131874314 missense variant G/C snv 0.800 1.000 7 2003 2016
dbSNP: rs140248167
rs140248167
ENPP1
1 1.000 0.040 6 131875849 missense variant A/G snv 1.2E-05 1.4E-05 0.700 1.000 7 2003 2016
dbSNP: rs147346173
rs147346173
ENPP1
1 1.000 0.040 6 131884949 missense variant A/G snv 1.2E-04 2.7E-04 0.700 1.000 7 2003 2016
dbSNP: rs148462924
rs148462924
ENPP1
1 1.000 0.040 6 131872076 missense variant A/C;G snv 4.0E-06; 8.8E-05 0.700 1.000 7 2003 2016
dbSNP: rs370184526
rs370184526
ENPP1
2 0.925 0.200 6 131884994 missense variant A/G snv 7.6E-05 6.3E-05 0.700 1.000 7 2003 2016
dbSNP: rs754659608
rs754659608
ENPP1
1 1.000 0.040 6 131858701 missense variant C/T snv 1.6E-05 7.0E-06 0.700 1.000 7 2003 2016
dbSNP: rs760786509
rs760786509
ENPP1
1 1.000 0.040 6 131854955 missense variant C/A snv 2.0E-05 0.700 1.000 7 2003 2016
dbSNP: rs763457176
rs763457176
ENPP1
1 1.000 0.040 6 131852201 missense variant T/C snv 1.6E-05 1.4E-05 0.700 1.000 7 2003 2016
dbSNP: rs764735802
rs764735802
ENPP1
1 1.000 0.040 6 131864526 missense variant G/A snv 8.0E-06 0.700 1.000 7 2003 2016
dbSNP: rs765071179
rs765071179
ENPP1
1 1.000 0.040 6 131869451 missense variant G/A snv 2.0E-05 7.0E-06 0.700 1.000 7 2003 2016
dbSNP: rs777367269
rs777367269
ENPP1
1 1.000 0.040 6 131877024 stop gained G/A;T snv 4.0E-06; 4.0E-06 0.700 1.000 7 2003 2016
dbSNP: rs121908248
rs121908248
ENPP1
2 0.925 0.200 6 131860388 missense variant G/C;T snv 0.700 0
dbSNP: rs121918023
rs121918023
ENPP1
1 1.000 0.040 6 131890410 stop gained G/T snv 0.700 0
dbSNP: rs1231182870
rs1231182870
ENPP1
1 1.000 0.040 6 131854961 missense variant A/T snv 7.0E-06 0.700 0
dbSNP: rs1243920034
rs1243920034
ENPP1
2 0.925 0.040 6 131873023 missense variant A/G snv 0.700 0
dbSNP: rs143393727
rs143393727
ENPP1
1 1.000 0.040 6 131879910 missense variant A/G snv 1.6E-05 4.2E-05 0.700 0
dbSNP: rs143771474
rs143771474
ENPP1
1 1.000 0.040 6 131860417 missense variant G/A snv 1.2E-05 5.6E-05 0.700 0
dbSNP: rs1554203715
rs1554203715
ENPP1
1 1.000 0.040 6 131864551 frameshift variant CAGCTTCCTAA/- delins 0.700 0
dbSNP: rs1562523328
rs1562523328
ENPP1
1 1.000 0.040 6 131861679 missense variant C/G snv 0.700 0
dbSNP: rs184483616
rs184483616
ENPP1
1 1.000 0.040 6 131890395 missense variant C/G;T snv 2.8E-05 0.700 0