Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs102275
TMEM258
0.827 0.320 11 61790331 non coding transcript exon variant T/C snv 0.47 10
rs174535
MYRF ; TMEM258
0.776 0.280 11 61783884 missense variant T/A;C;G snv 0.38 0.32 8
rs174537
TMEM258 ; MYRF
0.708 0.400 11 61785208 non coding transcript exon variant G/T snv 0.28 5
rs174534
MYRF ; TMEM258
1.000 0.080 11 61781986 non coding transcript exon variant A/G snv 0.28 3
rs412334
FEN1 ; TMEM258 ; MIR611
11 61792789 5 prime UTR variant C/T snv 0.10 2
rs509360
MYRF ; TMEM258
11 61781087 intron variant A/G snv 0.61 0.52 2
rs579383
MYRF ; TMEM258
11 61769111 intron variant G/A snv 0.58 2
rs149803
MYRF ; TMEM258
11 61771548 synonymous variant C/G;T snv 0.18 2
rs740006
TMEM258
11 61790396 3 prime UTR variant T/C snv 7.6E-02 2
rs174538
TMEM258 ; MIR611 ; FEN1
0.701 0.440 11 61792609 5 prime UTR variant G/A snv 0.34 0.26 2
rs174536
TMEM258 ; MYRF
11 61784455 non coding transcript exon variant A/C snv 0.29 2
rs2269928
TMEM258 ; MYRF
11 61770057 intron variant T/G snv 0.18 2
rs17762402
TMEM258 ; MYRF
11 61785729 intron variant G/A snv 4.8E-02 2
rs650436
TMEM258 ; MYRF
11 61768958 intron variant C/T snv 0.39 2
rs108499
TMEM258 ; MYRF
11 61779765 intron variant C/T snv 0.27 2
rs174532
TMEM258 ; MYRF
11 61781402 intron variant G/A snv 0.20 2
rs174528
TMEM258 ; MYRF
1.000 0.080 11 61776027 intron variant T/C snv 0.42 0.42 2
rs695867
FEN1 ; TMEM258 ; MIR611 ; FADS2
11 61793816 intron variant A/G snv 2.6E-02 1
rs7102974
MIR611 ; FEN1 ; TMEM258
11 61792563 5 prime UTR variant C/T snv 8.5E-03 9.6E-03 1
rs174530
MYRF ; TMEM258
1.000 0.080 11 61779120 non coding transcript exon variant A/G snv 0.30 1
rs174529
MYRF ; TMEM258
11 61776489 intron variant T/C snv 0.34 1
rs174533
MYRF ; TMEM258
0.763 0.160 11 61781553 intron variant G/A snv 0.37 0.29 1
rs7943728
MYRF ; TMEM258
1.000 0.080 11 61779596 intron variant G/A snv 0.12 0.11 1
rs628993
MYRF ; TMEM258
11 61772219 intron variant G/A snv 8.8E-02 1
rs61747222
MYRF ; TMEM258
11 61781324 missense variant G/A snv 2.2E-02 2.2E-02 1