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: rs80356476
rs80356476
2 0.925 0.040 2 166277252 missense variant G/A snv 0.810 1.000 12 2004 2014
dbSNP: rs80356469
rs80356469
2 0.925 0.080 2 166304279 missense variant A/G snv 0.800 1.000 11 2004 2014
dbSNP: rs80356470
rs80356470
1 1.000 0.040 2 166303270 missense variant A/T snv 0.800 1.000 11 2004 2014
dbSNP: rs80356471
rs80356471
1 1.000 0.040 2 166288566 missense variant G/A;C;T snv 0.800 1.000 11 2004 2014
dbSNP: rs80356474
rs80356474
4 0.925 0.040 2 166277281 missense variant A/G snv 0.800 1.000 11 2004 2014
dbSNP: rs80356475
rs80356475
1 1.000 0.040 2 166277251 missense variant A/T snv 0.800 1.000 11 2004 2014
dbSNP: rs80356478
rs80356478
1 1.000 0.040 2 166226587 missense variant A/C snv 0.800 1.000 11 2004 2014
dbSNP: rs267607030
rs267607030
1 1.000 0.040 2 166311728 missense variant T/C snv 1.3E-04 6.3E-05 0.700 1.000 11 2004 2014
dbSNP: rs879253994
rs879253994
2 0.925 0.080 2 166199711 missense variant G/A;T snv 4.0E-06 0.700 1.000 11 2004 2014
dbSNP: rs200945460
rs200945460
2 0.925 0.080 2 166280508 missense variant A/G;T snv 4.7E-06; 1.6E-04 0.700 1.000 3 2012 2016
dbSNP: rs80356468
rs80356468
1 1.000 0.040 2 166306571 missense variant T/C snv 0.700 0
dbSNP: rs80356473
rs80356473
1 1.000 0.040 2 166278156 missense variant A/C;G snv 4.0E-06 0.700 0
dbSNP: rs80356477
rs80356477
2 0.925 0.040 2 166277237 missense variant C/A;G snv 1.2E-05 0.700 0
dbSNP: rs6746030
rs6746030
16 0.763 0.320 2 166242648 missense variant A/G snv 0.88 0.88 0.010 1.000 1 2011 2011