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: rs121912548
rs121912548
MNX1 ; MNX1-AS2
1 1.000 0.120 7 157006595 missense variant T/A snv 0.800 1.000 4 2000 2012
dbSNP: rs121912546
rs121912546
MNX1 ; MNX1-AS2
1 1.000 0.120 7 157006556 stop gained G/A snv 0.700 0
dbSNP: rs121912547
rs121912547
MNX1 ; MNX1-AS1
1 1.000 0.120 7 157009859 stop gained G/A;T snv 0.700 0
dbSNP: rs121912549
rs121912549
MNX1 ; MNX1-AS2
1 1.000 0.120 7 157006487 stop gained C/A snv 0.700 0
dbSNP: rs1554594329
rs1554594329
MNX1 ; MNX1-AS1
1 1.000 0.120 7 157010297 frameshift variant -/G delins 0.700 0
dbSNP: rs1563700090
rs1563700090
MNX1 ; MNX1-AS2
1 1.000 0.120 7 157005875 splice acceptor variant T/C snv 0.700 0
dbSNP: rs1563700419
rs1563700419
MNX1 ; MNX1-AS2
1 1.000 0.120 7 157006478 splice donor variant C/T snv 0.700 0