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: rs968567
rs968567
7 0.851 0.240 11 61828092 intron variant C/T snv 0.11 0.700 1.000 1 2011 2011
dbSNP: rs174570
rs174570
11 0.882 0.200 11 61829740 intron variant C/T snv 0.15 0.700 1.000 1 2011 2011
dbSNP: rs174550
rs174550
13 0.925 0.160 11 61804006 5 prime UTR variant T/C snv 0.28 0.700 1.000 1 2011 2011
dbSNP: rs174556
rs174556
7 0.925 0.160 11 61813163 intron variant C/T snv 0.26 0.700 1.000 1 2011 2011
dbSNP: rs174541
rs174541
8 1.000 0.080 11 61798436 intron variant T/C snv 0.29 0.700 1.000 1 2011 2011
dbSNP: rs174574
rs174574
7 1.000 0.080 11 61832870 intron variant A/C snv 0.55 0.700 1.000 1 2011 2011
dbSNP: rs174575
rs174575
3 1.000 0.040 11 61834531 intron variant C/G snv 0.25 0.700 1.000 1 2011 2011
dbSNP: rs174602
rs174602
3 1.000 0.080 11 61856942 non coding transcript exon variant T/C snv 0.37 0.700 1.000 1 2011 2011
dbSNP: rs174616
rs174616
3 1.000 0.080 11 61861650 intron variant G/A snv 0.51 0.700 1.000 1 2011 2011
dbSNP: rs2072114
rs2072114
4 1.000 0.080 11 61837743 intron variant A/G snv 0.19 0.16 0.700 1.000 1 2011 2011
dbSNP: rs2845573
rs2845573
3 1.000 0.040 11 61834436 intron variant A/G snv 9.7E-02 0.700 1.000 1 2011 2011
dbSNP: rs498793
rs498793
3 1.000 0.040 11 61857233 intron variant T/C snv 0.62 0.700 1.000 1 2011 2011
dbSNP: rs526126
rs526126
3 1.000 0.040 11 61857413 intron variant G/C;T snv 0.81; 8.0E-06 0.700 1.000 1 2011 2011