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: rs11737218
rs11737218
1 1.000 0.040 4 26884151 intron variant G/T snv 0.29 0.700 1.000 1 2017 2017
dbSNP: rs12641141
rs12641141
1 1.000 0.040 4 26911569 intron variant C/A snv 1.9E-02 0.700 1.000 1 2017 2017
dbSNP: rs12644073
rs12644073
1 1.000 0.040 4 26895436 intron variant C/T snv 0.30 0.700 1.000 1 2017 2017
dbSNP: rs13108758
rs13108758
1 1.000 0.040 4 26898151 intron variant A/G snv 2.5E-02 0.700 1.000 1 2017 2017
dbSNP: rs4129747
rs4129747
1 1.000 0.040 4 26891234 intron variant G/A snv 4.0E-02 0.700 1.000 1 2017 2017
dbSNP: rs4692129
rs4692129
1 1.000 0.040 4 26865089 intron variant T/C snv 0.84 0.700 1.000 1 2017 2017
dbSNP: rs4692132
rs4692132
1 1.000 0.040 4 26888810 intron variant A/G snv 0.51 0.700 1.000 1 2017 2017
dbSNP: rs6833053
rs6833053
1 1.000 0.040 4 26870838 intron variant G/A snv 0.28 0.700 1.000 1 2017 2017
dbSNP: rs6855521
rs6855521
1 1.000 0.040 4 26884584 intron variant C/A snv 0.19 0.700 1.000 1 2017 2017
dbSNP: rs7672936
rs7672936
1 1.000 0.040 4 26882786 intron variant C/T snv 0.64 0.700 1.000 1 2017 2017
dbSNP: rs9654110
rs9654110
1 1.000 0.040 4 26911472 intron variant C/G snv 0.49 0.700 1.000 1 2017 2017
dbSNP: rs9998368
rs9998368
1 1.000 0.040 4 26887432 intron variant C/T snv 0.62 0.700 1.000 1 2017 2017