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: rs1960278
rs1960278
2 0.925 0.160 6 31302097 intron variant C/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs2213140
rs2213140
1 1.000 0.040 6 31293408 intron variant T/C snv 0.66 0.700 1.000 1 2012 2012
dbSNP: rs2243866
rs2243866
1 1.000 0.040 6 31293419 intron variant G/A snv 0.66 0.700 1.000 1 2012 2012
dbSNP: rs2243868
rs2243868
2 0.925 0.160 6 31293499 intron variant A/G snv 0.66 0.700 1.000 1 2012 2012
dbSNP: rs2246954
rs2246954
2 0.925 0.160 6 31297485 intron variant A/G snv 0.60 0.700 1.000 1 2012 2012
dbSNP: rs2247056
rs2247056
11 0.882 0.160 6 31297713 intron variant T/C snv 0.80 0.700 1.000 1 2012 2012
dbSNP: rs2524060
rs2524060
2 0.925 0.120 6 31299645 intron variant A/C;T snv 0.700 1.000 1 2012 2012
dbSNP: rs2524066
rs2524066
2 0.925 0.160 6 31301377 intron variant T/C snv 0.65 0.700 1.000 1 2012 2012
dbSNP: rs2524129
rs2524129
1 1.000 0.040 6 31297358 intron variant C/G snv 0.80 0.700 1.000 1 2012 2012
dbSNP: rs2524139
rs2524139
2 1.000 0.040 6 31296356 intron variant G/C;T snv 0.700 1.000 1 2012 2012
dbSNP: rs2524142
rs2524142
2 1.000 0.040 6 31295745 intron variant C/A;G snv 0.700 1.000 1 2012 2012
dbSNP: rs2524143
rs2524143
2 1.000 0.040 6 31295733 intron variant T/C snv 0.81 0.700 1.000 1 2012 2012
dbSNP: rs2853918
rs2853918
2 0.925 0.160 6 31300843 intron variant C/T snv 0.65 0.700 1.000 1 2012 2012
dbSNP: rs2853921
rs2853921
1 1.000 0.040 6 31299284 intron variant A/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs2853922
rs2853922
1 1.000 0.040 6 31298413 intron variant A/G snv 0.65 0.700 1.000 1 2012 2012