Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs193302982 | 1.000 | 0.080 | MT | 14783 | synonymous variant | T/C | snv | 1 | |||
rs193302983 | 1.000 | 0.080 | MT | 14905 | synonymous variant | G/A | snv | 1 | |||
rs193302985 | 1.000 | 0.080 | MT | 15043 | synonymous variant | G/A | snv | 1 | |||
rs193302991 | 1.000 | 0.080 | MT | 15301 | synonymous variant | G/A | snv | 1 | |||
rs386419981 | 1.000 | 0.080 | MT | 14891 | missense variant | C/G | snv | 1 | |||
rs527236164 | 1.000 | 0.080 | MT | 14800 | synonymous variant | C/T | snv | 1 | |||
rs527236166 | 1.000 | 0.080 | MT | 14950 | synonymous variant | C/T | snv | 1 | |||
rs527236167 | 1.000 | 0.080 | MT | 14968 | synonymous variant | T/C | snv | 1 | |||
rs527236168 | 1.000 | 0.080 | MT | 14974 | synonymous variant | C/G;T | snv | 1 | |||
rs527236169 | 1.000 | 0.080 | MT | 15001 | synonymous variant | T/C | snv | 1 | |||
rs527236170 | 1.000 | 0.080 | MT | 15049 | synonymous variant | C/T | snv | 1 | |||
rs527236173 | 1.000 | 0.080 | MT | 15214 | synonymous variant | T/C | snv | 1 | |||
rs527236174 | 1.000 | 0.080 | MT | 15226 | synonymous variant | A/G | snv | 1 | |||
rs527236175 | 1.000 | 0.080 | MT | 15289 | synonymous variant | T/C | snv | 1 | |||
rs527236180 | 1.000 | 0.080 | MT | 15346 | synonymous variant | G/A | snv | 1 | |||
rs527236181 | 1.000 | 0.080 | MT | 15355 | synonymous variant | G/A | snv | 1 | |||
rs527236183 | 1.000 | 0.080 | MT | 15385 | synonymous variant | C/T | snv | 1 | |||
rs527236189 | 1.000 | 0.080 | MT | 15553 | synonymous variant | G/A | snv | 1 | |||
rs527236190 | 1.000 | 0.080 | MT | 15637 | synonymous variant | C/T | snv | 1 | |||
rs527236191 | 1.000 | 0.080 | MT | 15649 | synonymous variant | A/G | snv | 1 | |||
rs527236192 | 1.000 | 0.080 | MT | 15682 | synonymous variant | A/G | snv | 1 | |||
rs527236194 | 1.000 | 0.080 | MT | 15784 | synonymous variant | T/C | snv | 1 | |||
rs527236201 | 1.000 | 0.080 | MT | 15349 | missense variant | C/A;T | snv | 1 | |||
rs527236202 | 1.000 | 0.080 | MT | 14732 | non coding transcript exon variant | A/G | snv | 1 | |||
rs527236204 | 1.000 | 0.080 | MT | 14935 | synonymous variant | T/C | snv | 1 |