Source: ALL
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs587777491
rs587777491
HCN1
1 1.000 5 45396521 missense variant C/G snv 0.800 1.000 3 2014 2018
dbSNP: rs587777492
rs587777492
HCN1
1 1.000 5 45695795 missense variant G/A snv 8.1E-06 0.800 1.000 3 2014 2018
dbSNP: rs587777493
rs587777493
HCN1
1 1.000 5 45645220 missense variant A/G snv 0.800 1.000 3 2014 2018
dbSNP: rs587777494
rs587777494
HCN1
1 1.000 5 45461967 missense variant C/G;T snv 4.0E-06 0.800 1.000 3 2014 2018
dbSNP: rs587777495
rs587777495
HCN1
1 1.000 5 45645199 missense variant G/A snv 0.800 1.000 3 2014 2018
dbSNP: rs1057519547
rs1057519547
HCN1
2 0.925 0.040 5 45396550 missense variant C/T snv 0.800 0
dbSNP: rs1057519548
rs1057519548
HCN1
2 0.925 0.040 5 45645575 missense variant C/G snv 0.800 0
dbSNP: rs544994462
rs544994462
HCN1
1 1.000 5 45695954 missense variant C/A snv 6.6E-03 3.6E-03 0.700 1.000 3 2014 2018
dbSNP: rs1554040120
rs1554040120
HCN1
1 1.000 5 45695680 frameshift variant G/- del 0.700 0