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: rs201992075
rs201992075
CHD4 ; SCARNA11
1 1.000 12 6581131 missense variant C/G;T snv 4.0E-06; 3.6E-05 4.9E-05 0.800 0
dbSNP: rs886039915
rs886039915
CHD4
3 0.925 12 6591713 missense variant C/T snv 0.800 0
dbSNP: rs886039916
rs886039916
CHD4
1 1.000 12 6593191 missense variant G/T snv 0.800 0
dbSNP: rs886039917
rs886039917
CHD4
1 1.000 12 6588383 missense variant C/T snv 0.800 0
dbSNP: rs886039918
rs886039918
CHD4
1 1.000 12 6587897 missense variant C/A snv 0.800 0
dbSNP: rs886039919
rs886039919
CHD4
1 1.000 12 6588320 missense variant C/A snv 0.800 0
dbSNP: rs1060499583
rs1060499583
CHD4
1 1.000 12 6587518 missense variant A/C snv 0.700 0