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: rs3803369
rs3803369
TNFAIP8L3 ; MIR4713HG
2 0.925 0.040 15 51083632 intron variant T/A;C snv 0.010 1.000 1 2008 2008
dbSNP: rs6701216
rs6701216
LCE1C
2 0.925 0.040 1 152806050 intron variant C/T snv 0.21 0.010 1.000 1 2008 2008
dbSNP: rs7993214
rs7993214
COG6
2 0.925 0.040 13 39776775 intron variant T/C;G snv 0.010 1.000 1 2008 2008