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: rs1217691063
rs1217691063
614 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 0.100 0.923 52 1999 2019
dbSNP: rs397507444
rs397507444
306 0.405 0.880 1 11794407 missense variant T/G snv 0.100 0.909 11 2006 2018
dbSNP: rs1801133
rs1801133
174 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 0.070 1.000 7 2004 2018
dbSNP: rs1801131
rs1801131
93 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 0.020 1.000 2 2016 2019
dbSNP: rs765625943
rs765625943
4 0.882 0.200 1 11803417 missense variant G/A snv 4.3E-06 0.020 1.000 2 2016 2016
dbSNP: rs142884651
rs142884651
1 1.000 0.080 1 11786327 3 prime UTR variant G/A snv 0.010 1.000 1 2018 2018
dbSNP: rs4846048
rs4846048
10 0.752 0.280 1 11786195 3 prime UTR variant G/A snv 0.67 0.010 1.000 1 2017 2017
dbSNP: rs868014
rs868014
1 1.000 0.080 1 11789390 missense variant A/G snv 0.99 0.94 0.010 1.000 1 2017 2017