Gene: MED12L ×
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: rs1559855453
rs1559855453
MED12L
1 3 151188468 frameshift variant -/C delins 0.700 0
dbSNP: rs1560103306
rs1560103306
P2RY12 ; MED12L
1 3 151380116 missense variant G/A snv 0.700 0
dbSNP: rs1560108090
rs1560108090
P2RY12 ; MED12L
1 3 151384082 splice acceptor variant G/A snv 0.700 0
dbSNP: rs1560115921
rs1560115921
MED12L
1 3 151390003 stop gained C/T snv 0.700 0