Gene: CHD7 ×
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: rs13277976
rs13277976
CHD7
1 8 60766479 intron variant A/T snv 0.77 0.700 1.000 1 2016 2016
dbSNP: rs35914442
rs35914442
CHD7
2 8 60724328 intron variant A/G snv 0.17 0.700 1.000 1 2016 2016
dbSNP: rs4449834
rs4449834
CHD7
2 8 60843309 intron variant G/T snv 0.71 0.700 1.000 1 2016 2016
dbSNP: rs6994642
rs6994642
CHD7
1 8 60811218 intron variant C/T snv 0.18 0.700 1.000 1 2018 2018
dbSNP: rs7842389
rs7842389
CHD7
1 8 60772635 intron variant C/T snv 0.77 0.700 1.000 1 2019 2019
dbSNP: rs7846314
rs7846314
CHD7
5 8 60738272 intron variant A/T snv 0.27 0.700 1.000 1 2016 2016