Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11074967
LOC105371082 ; LOC400499 ; RMI2
0.807 0.120 16 11377557 intron variant C/G snv 0.36 6
rs367569
LOC105371082 ; RMI2
0.807 0.120 16 11271643 intron variant C/T snv 0.32 6
rs8061370
LOC105371082 ; RMI2
0.882 16 11364614 intron variant A/C;T snv 4
rs529866
LOC105371082 ; RMI2
1.000 0.040 16 11279463 intron variant C/T snv 0.18 2
rs423674
RMI2 ; LOC105371082
0.925 0.120 16 11279548 intron variant G/T snv 0.18 2
rs11643024
RMI2 ; LOC105371082
16 11349326 intron variant A/G snv 0.67 2
rs4780355
SOCS1 ; RMI2 ; LOC105371082
0.882 0.120 16 11254001 intron variant T/C;G snv 2
rs12928822
LOC105371082 ; RMI2
0.882 0.200 16 11310036 intron variant C/T snv 0.13 1
rs1646019
LOC105371082 ; RMI2
1.000 0.080 16 11265823 intron variant C/T snv 0.36 1
rs7188861
LOC105371082 ; RMI2
16 11360793 intron variant C/A snv 0.16 1
rs193778
LOC105371082 ; SOCS1 ; RMI2
1.000 0.120 16 11257354 intron variant A/G snv 0.20 1
rs6498184
LOC105371083 ; RMI2 ; LOC105371082
1.000 0.080 16 11342133 non coding transcript exon variant T/A;C snv 1
rs35578928
LOC400499 ; LOC105371082 ; RMI2
16 11373920 intron variant G/A snv 0.15 1
rs80073729
RMI2 ; LOC105371082
1.000 0.080 16 11279940 intron variant G/A snv 4.1E-03 1
rs77804393
RMI2 ; LOC105371082
1.000 0.040 16 11265296 intron variant G/A;T snv 1
rs77061563
RMI2 ; LOC105371082
1.000 0.040 16 11358685 intron variant C/G;T snv 1
rs7191700
RMI2 ; LOC105371082
1.000 0.080 16 11312946 intron variant C/T snv 0.27 1
rs4781072
RMI2 ; LOC105371082
16 11366623 intron variant C/G;T snv 1
rs11549428
SOCS1 ; RMI2 ; LOC105371082
16 11254849 missense variant C/G;T snv 5.0E-03 1