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 0.938 32 1999 2019
dbSNP: rs397507444
rs397507444
306 0.405 0.880 1 11794407 missense variant T/G snv 0.090 0.889 9 2000 2017
dbSNP: rs1801133
rs1801133
174 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 0.050 0.800 5 2012 2019
dbSNP: rs1801131
rs1801131
93 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 0.020 1.000 2 2014 2014
dbSNP: rs12121543
rs12121543
4 0.851 0.240 1 11794614 intron variant C/A snv 0.21 0.010 1.000 1 2014 2014
dbSNP: rs13306553
rs13306553
3 0.882 0.160 1 11800060 non coding transcript exon variant A/G snv 9.9E-02 0.010 1.000 1 2014 2014
dbSNP: rs2274976
rs2274976
7 0.807 0.320 1 11790870 missense variant C/T snv 5.6E-02 4.2E-02 0.010 1.000 1 2014 2014
dbSNP: rs9651118
rs9651118
20 0.683 0.480 1 11802157 intron variant T/C snv 0.18 0.010 1.000 1 2014 2014