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: rs104894446
rs104894446
MGAT2 ; RPL36AL
1 1.000 0.120 14 49622137 missense variant C/T snv 0.800 1.000 2 1996 2000
dbSNP: rs104894447
rs104894447
MGAT2 ; RPL36AL
1 1.000 0.120 14 49622053 missense variant A/G snv 0.800 1.000 2 1996 2000
dbSNP: rs104894448
rs104894448
MGAT2 ; RPL36AL
1 1.000 0.120 14 49622220 missense variant A/G snv 0.800 1.000 2 1996 2000
dbSNP: rs104894449
rs104894449
MGAT2 ; RPL36AL
1 1.000 0.120 14 49622285 stop gained T/A snv 0.700 0
dbSNP: rs1310787426
rs1310787426
MGAT2 ; RPL36AL
1 1.000 0.120 14 49621359 stop gained C/T snv 4.1E-06 7.0E-06 0.700 0
dbSNP: rs1566504935
rs1566504935
MGAT2 ; RPL36AL
1 1.000 0.120 14 49622020 frameshift variant -/T delins 0.700 0
dbSNP: rs1566505013
rs1566505013
MGAT2 ; RPL36AL
1 1.000 0.120 14 49622067 missense variant G/C snv 0.700 0
dbSNP: rs730882218
rs730882218
MGAT2 ; RPL36AL
3 0.925 0.120 14 49621979 missense variant G/C snv 0.700 0
dbSNP: rs776531113
rs776531113
MGAT2 ; RPL36AL
1 1.000 0.120 14 49622388 missense variant C/T snv 4.0E-06 1.4E-05 0.700 0