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: rs2715148
rs2715148
1 1.000 0.040 7 82820719 3 prime UTR variant A/C snv 0.57 0.800 1.000 2 2009 2011
dbSNP: rs2522833
rs2522833
7 0.827 0.080 7 82824392 missense variant A/C snv 0.45 0.34 0.780 1.000 9 2009 2017
dbSNP: rs2715157
rs2715157
1 1.000 0.040 7 82839058 intron variant A/G;T snv 0.710 1.000 1 2017 2017
dbSNP: rs2247523
rs2247523
1 1.000 0.040 7 82825088 intron variant C/G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs2522840
rs2522840
1 1.000 0.040 7 82849099 intron variant T/G snv 0.38 0.700 1.000 1 2009 2009
dbSNP: rs6954078
rs6954078
1 1.000 0.040 7 82806562 intron variant G/T snv 0.48 0.700 1.000 1 2009 2009