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: rs10246939
rs10246939
TAS2R38 ; MGAM
6 0.851 0.240 7 141972804 missense variant T/C snv 0.49 0.47 0.700 1.000 1 2011 2011
dbSNP: rs11762634
rs11762634
MGAM
1 7 141956687 intron variant G/A snv 0.22 0.700 1.000 1 2011 2011
dbSNP: rs11767119
rs11767119
MGAM
1 7 141912316 intron variant G/A snv 0.23 0.700 1.000 1 2011 2011
dbSNP: rs11767947
rs11767947
MGAM
1 7 141912821 intron variant G/A snv 0.23 0.700 1.000 1 2011 2011
dbSNP: rs12539499
rs12539499
MGAM ; CLEC5A
1 7 141930467 intron variant T/C snv 0.23 0.700 1.000 1 2011 2011
dbSNP: rs17162635
rs17162635
MGAM
1 7 141978163 intron variant T/A snv 1.0E-01 0.700 1.000 1 2011 2011
dbSNP: rs1726866
rs1726866
TAS2R38 ; MGAM
3 0.925 0.120 7 141972905 missense variant G/A snv 0.50 0.47 0.700 1.000 1 2011 2011
dbSNP: rs4725559
rs4725559
AGK
1 7 141587852 intron variant G/A snv 0.36 0.700 1.000 1 2011 2011
dbSNP: rs4726463
rs4726463
DENND11
1 7 141666839 intron variant A/G snv 0.35 0.700 1.000 1 2011 2011
dbSNP: rs4726481
rs4726481
MGAM
1 7 141968603 intron variant G/T snv 0.43 0.700 1.000 1 2011 2011
dbSNP: rs6976028
rs6976028
MGAM
1 7 141912917 intron variant C/T snv 0.25 0.700 1.000 1 2011 2011
dbSNP: rs713598
rs713598
TAS2R38 ; MGAM
7 0.851 0.160 7 141973545 missense variant C/G snv 0.46 0.44 0.700 1.000 1 2011 2011