Source: UNIPROT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs74315511
NCAPH2 ; SCO2
0.925 0.240 22 50523994 missense variant C/T snv 8.0E-05 1.1E-04 2
rs759452074
SCO2 ; NCAPH2
0.925 0.200 22 50523835 missense variant C/A;T snv 8.0E-06; 3.2E-05 2
rs1352878283
NCAPH2 ; SCO2
1.000 0.120 22 50523639 missense variant A/G snv 7.0E-06 1
rs370130010
NCAPH2 ; SCO2
1.000 0.040 22 50524078 missense variant G/A;T snv 4.8E-05 1
rs375954523
SCO2 ; NCAPH2
1.000 0.040 22 50524054 missense variant G/A;T snv 8.0E-05; 4.0E-06 1
rs145100473
SCO2 ; NCAPH2
1.000 0.040 22 50524071 missense variant C/T snv 8.3E-04 7.6E-04 1
rs8139305
SCO2 ; NCAPH2
1.000 0.040 22 50523636 missense variant G/A;T snv 2.4E-03; 4.0E-06 1
rs28937868
SCO2 ; NCAPH2
1.000 0.200 22 50524014 missense variant C/T snv 1
rs28937598
SCO2 ; NCAPH2
1.000 0.200 22 50523901 missense variant G/A snv 1.2E-05 7.0E-06 1
rs80358232
SCO2 ; NCAPH2
1.000 0.200 22 50523738 missense variant G/A;T snv 4.0E-06 1
rs149977726
SCO2 ; TYMP
1.000 22 50527265 missense variant T/C snv 1.2E-05 9.8E-05 1