Gene: HCN4 ×
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: rs7164883
rs7164883
HCN4
1 1.000 0.080 15 73359833 intron variant A/G snv 0.21 0.820 1.000 3 2012 2019
dbSNP: rs1457768351
rs1457768351
HCN4
1 1.000 0.080 15 73367502 missense variant G/A snv 0.010 1.000 1 2014 2014
dbSNP: rs148398509
rs148398509
HCN4
5 0.882 0.160 15 73323445 missense variant G/C snv 7.8E-03 7.2E-03 0.010 1.000 1 2019 2019
dbSNP: rs498005
rs498005
HCN4
5 0.851 0.160 15 73327969 intron variant C/T snv 0.48 0.010 1.000 1 2019 2019