Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs397516248
MYH7 ; MHRT
0.851 0.200 14 23415153 missense variant C/T snv 6
rs367543052
MHRT ; MYH7
0.882 0.160 14 23415476 inframe deletion TCT/-;TCTTCT delins 4