| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs199473072 | 0.827 | 0.160 | 3 | 38613773 | missense variant | G/A | snv | 1.2E-05 | 8.4E-05 | 3 | |
| rs199473074 | 1.000 | 0.080 | 3 | 38613758 | missense variant | T/C | snv | 4.2E-06 | 1 | ||
| rs199473076 | 0.925 | 0.120 | 3 | 38609950 | missense variant | C/T | snv | 8.0E-06 | 2.8E-05 | 2 | |
| rs199473077 | 1.000 | 0.120 | 3 | 38609935 | missense variant | G/T | snv | 8.0E-06 | 7.0E-06 | 1 | |
| rs199473078 | 1.000 | 0.120 | 3 | 38609929 | missense variant | C/G | snv | 5.6E-05 | 4.2E-05 | 1 | |
| rs199473079 | 1.000 | 0.080 | 3 | 38609860 | missense variant | G/T | snv | 1 | |||
| rs199473080 | 1.000 | 0.120 | 3 | 38609843 | missense variant | G/T | snv | 1 | |||
| rs199473081 | 1.000 | 0.080 | 3 | 38609841 | missense variant | A/T | snv | 1 | |||
| rs199473082 | 1.000 | 0.080 | 3 | 38609824 | missense variant | G/A;C | snv | 1 | |||
| rs199473083 | 0.925 | 0.080 | 3 | 38609823 | missense variant | C/T | snv | 1.6E-05 | 1 | ||
| rs199473084 | 1.000 | 0.120 | 3 | 38609803 | missense variant | C/G;T | snv | 1.6E-05 | 1 | ||
| rs199473086 | 1.000 | 0.080 | 3 | 38609788 | missense variant | C/T | snv | 4.0E-06; 2.4E-05 | 3.5E-05 | 1 | |
| rs199473088 | 1.000 | 0.080 | 3 | 38609770 | missense variant | C/T | snv | 4.0E-06 | 1.4E-05 | 1 | |
| rs199473090 | 1.000 | 0.080 | 3 | 38608194 | missense variant | C/A;G;T | snv | 4.0E-06; 4.0E-06; 4.8E-05 | 1 | ||
| rs199473091 | 1.000 | 0.080 | 3 | 38608190 | missense variant | G/T | snv | 8.0E-06 | 1 | ||
| rs199473092 | 0.925 | 0.080 | 3 | 38608175 | missense variant | A/C | snv | 1 | |||
| rs199473093 | 0.925 | 0.080 | 3 | 38606802 | missense variant | G/A | snv | 1 | |||
| rs199473094 | 1.000 | 0.120 | 3 | 38606791 | missense variant | G/A | snv | 4.0E-06 | 7.0E-06 | 1 | |
| rs199473095 | 1.000 | 0.080 | 3 | 38606757 | missense variant | C/A;T | snv | 1 | |||
| rs199473096 | 0.882 | 0.120 | 3 | 38606751 | missense variant | G/A | snv | 1 | |||
| rs199473097 | 0.763 | 0.120 | 3 | 38606710 | missense variant | G/A | snv | 8.0E-06 | 7.0E-06 | 2 | |
| rs199473098 | 1.000 | 0.080 | 3 | 38606703 | missense variant | A/T | snv | 1 | |||
| rs199473099 | 1.000 | 0.120 | 3 | 38606700 | missense variant | G/A | snv | 1 | |||
| rs199473101 | 0.925 | 0.080 | 3 | 38606682 | missense variant | C/A;T | snv | 8.1E-06 | 1 | ||
| rs199473102 | 1.000 | 0.080 | 3 | 38606133 | missense variant | C/T | snv | 1 |