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: rs756045117
rs756045117
3 0.925 0.080 3 37012090 missense variant C/G;T snv 1.6E-05 0.020 1.000 2 2007 2015
dbSNP: rs1799977
rs1799977
28 0.662 0.440 3 37012077 missense variant A/C;G;T snv 0.23 0.050 0.800 5 2007 2017
dbSNP: rs1224959447
rs1224959447
1 1.000 0.080 3 37050622 missense variant C/G snv 7.0E-06 0.010 1.000 1 2018 2018
dbSNP: rs63750242
rs63750242
1 1.000 0.080 3 37048941 missense variant T/C;G snv 0.010 1.000 1 2018 2018
dbSNP: rs63750977
rs63750977
1 1.000 0.080 3 37007031 missense variant C/G snv 0.010 1.000 1 2018 2018
dbSNP: rs63751467
rs63751467
2 0.925 0.120 3 37020438 missense variant A/G snv 9.2E-05 5.6E-05 0.010 1.000 1 2018 2018
dbSNP: rs1800734
rs1800734
30 0.653 0.400 3 36993455 5 prime UTR variant G/A snv 0.22 0.090 0.778 9 2010 2019