Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs174533
MYRF ; TMEM258
0.763 0.160 11 61781553 intron variant G/A snv 0.37 0.29 17
rs174537
TMEM258 ; MYRF
0.708 0.400 11 61785208 non coding transcript exon variant G/T snv 0.28 14
rs174535
MYRF ; TMEM258
0.776 0.280 11 61783884 missense variant T/A;C;G snv 0.38 0.32 11
rs174529
MYRF ; TMEM258
11 61776489 intron variant T/C snv 0.34 6
rs174530
MYRF ; TMEM258
1.000 0.080 11 61779120 non coding transcript exon variant A/G snv 0.30 3
rs174528
TMEM258 ; MYRF
1.000 0.080 11 61776027 intron variant T/C snv 0.42 0.42 3
rs2071213
MYRF
0.925 0.080 11 61766538 non coding transcript exon variant C/T snv 0.37 2
rs11320420
MYRF ; TMEM258
1.000 0.080 11 61774535 intron variant AAAAA/-;AAA;AAAA;AAAAAA delins 0.30 2
rs7943728
MYRF ; TMEM258
1.000 0.080 11 61779596 intron variant G/A snv 0.12 0.11 2
rs2956395
MYRF-AS1 ; MYRF
1.000 0.040 11 61752514 intron variant C/A;G snv 1
rs509360
MYRF ; TMEM258
11 61781087 intron variant A/G snv 0.61 0.52 1
rs61896141
MYRF ; TMEM258
11 61788567 intron variant A/C snv 0.11 1
rs174536
TMEM258 ; MYRF
11 61784455 non coding transcript exon variant A/C snv 0.29 1