Source: UNIPROT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1029888196
ACE2 ; BMX
1.000 0.080 X 15556127 missense variant C/T snv 5.7E-06 9.5E-06 1
rs1239950009
CAMK4
1.000 0.080 5 111484451 missense variant C/G snv 1
rs147940573
LMTK2
1.000 0.080 7 98191915 missense variant G/A;C snv 7.6E-05; 2.4E-05 1
rs370187232
MYO18B
1.000 0.080 22 25772410 missense variant C/T snv 7.6E-05 2.0E-04 1
rs780180192
MYO18B
1.000 0.080 22 26027636 missense variant C/G;T snv 4.0E-06; 8.9E-05 1
rs753661271
TRRAP
1.000 0.080 7 98976613 missense variant C/T snv 4.0E-06 1
rs1383995916
TTN-AS1 ; TTN
1.000 0.080 2 178589623 missense variant A/T snv 7.0E-06 1