Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs780571007
EFHC1
1.000 0.040 6 52454113 missense variant A/G snv 3.2E-05 5.6E-05 1
rs137852778
EFHC1
1.000 0.040 6 52454128 missense variant G/A;T snv 2.0E-05 1
rs1570624
EFHC1
0.882 0.040 6 52454252 missense variant G/A snv 1.0E-02 9.6E-03 3
rs527295360
EFHC1
1.000 0.040 6 52465035 missense variant C/T snv 2.1E-04 1.5E-04 1
rs767833659
EFHC1
1.000 0.040 6 52465042 missense variant A/G snv 4.0E-06 1
rs371151471
EFHC1
1.000 0.040 6 52465092 missense variant C/T snv 1.2E-03 2.0E-04 1
rs377286138
EFHC1
1.000 0.040 6 52479064 missense variant C/T snv 1.1E-04 7.0E-05 1
rs779322943
EFHC1
1.000 0.040 6 52479211 missense variant T/C snv 4.0E-06 1
rs534797617
EFHC1
1.000 0.040 6 52479212 missense variant A/C;G snv 1.6E-05 1
rs527539103
EFHC1
1.000 0.040 6 52479703 missense variant A/G snv 1
rs149998588
EFHC1
1.000 0.040 6 52479759 stop gained C/T snv 3.2E-05 1.4E-05 1
rs772265107
EFHC1
1.000 0.040 6 52490165 missense variant G/A;T snv 4.8E-05; 4.0E-06 1
rs17851770
EFHC1
1.000 0.040 6 52492273 missense variant A/C snv 6.2E-02 6.2E-02 1
rs142458862
EFHC1
1.000 0.040 6 52492274 missense variant T/G snv 1.8E-04 1.2E-04 1
rs574948354
EFHC1
1.000 0.040 6 52492310 missense variant A/G snv 8.0E-05 1
rs765078446
CILK1
0.925 0.040 6 53013900 missense variant T/G snv 2.0E-05 2.1E-05 3
rs9349688
LRRC1
1.000 0.040 6 53897294 missense variant A/G;T snv 0.12; 5.2E-05 1
rs772145901
HCN2
1.000 0.040 19 603647 missense variant G/A;C snv 1.6E-05; 8.0E-06 1
rs3752158
HCN2
1.000 0.040 19 607984 synonymous variant G/A;C snv 1.5E-03; 9.3E-02 1
rs183899632
CPA6
1.000 0.040 8 67746023 missense variant C/A;T snv 5.6E-05; 4.0E-05 1
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214