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: rs1371429276
rs1371429276
1 1.000 0.080 20 42472359 missense variant G/A snv 1.4E-05 0.700 0
dbSNP: rs63749803
rs63749803
1 1.000 0.080 3 37004421 missense variant T/C;G snv 0.700 0
dbSNP: rs63750297
rs63750297
1 1.000 0.080 3 37004412 missense variant C/A;G;T snv 8.0E-06 0.700 0
dbSNP: rs63750623
rs63750623
4 0.925 0.160 2 47480707 stop gained C/G;T snv 0.700 0
dbSNP: rs63750709
rs63750709
2 0.925 0.160 2 47480846 missense variant C/G;T snv 4.0E-06 0.700 0
dbSNP: rs63750795
rs63750795
1 1.000 0.080 2 47480854 missense variant T/G snv 0.700 0
dbSNP: rs63750966
rs63750966
1 1.000 0.080 2 47403240 missense variant G/A;C;T snv 0.700 0
dbSNP: rs63751047
rs63751047
1 1.000 0.080 3 37048525 missense variant C/A;G snv 0.700 0
dbSNP: rs63751400
rs63751400
1 1.000 0.080 2 47480839 missense variant C/G;T snv 4.0E-06 0.700 0
dbSNP: rs768678989
rs768678989
MET
1 1.000 0.080 7 116771932 missense variant C/T snv 2.8E-05 0.700 0
dbSNP: rs771333219
rs771333219
MET
1 1.000 0.080 7 116759444 missense variant C/T snv 1.2E-04 8.4E-05 0.700 0
dbSNP: rs780759537
rs780759537
1 1.000 0.080 16 68822082 missense variant G/A snv 1.6E-05 4.2E-05 0.700 0
dbSNP: rs10004195
rs10004195
8 0.790 0.320 4 38783103 upstream gene variant T/A snv 0.29 0.010 1.000 1 2015 2015
dbSNP: rs10022537
rs10022537
2 0.925 0.080 4 16075214 intron variant A/T snv 0.70 0.010 1.000 1 2015 2015
dbSNP: rs10052016
rs10052016
2 0.925 0.080 5 1427996 intron variant A/G snv 0.22 0.010 1.000 1 2013 2013
dbSNP: rs10052657
rs10052657
7 0.807 0.120 5 59111944 intron variant C/A snv 0.17 0.010 1.000 1 2018 2018
dbSNP: rs10088390
rs10088390
2 0.925 0.080 8 41264249 3 prime UTR variant C/G snv 0.19 0.010 1.000 1 2017 2017
dbSNP: rs1011445550
rs1011445550
2 0.925 0.080 17 7676391 missense variant G/C snv 0.010 1.000 1 2011 2011
dbSNP: rs10116253
rs10116253
4 0.851 0.120 9 117702042 upstream gene variant T/C snv 0.28 0.010 1.000 1 2014 2014
dbSNP: rs1016343
rs1016343
8 0.807 0.240 8 127081052 non coding transcript exon variant C/T snv 0.20 0.010 1.000 1 2019 2019
dbSNP: rs1042028
rs1042028
30 0.658 0.440 16 28606193 missense variant C/T snv 0.22 0.30 0.010 1.000 1 2005 2005
dbSNP: rs10421916
rs10421916
2 0.925 0.080 19 17818178 intron variant A/G snv 0.69 0.010 1.000 1 2012 2012
dbSNP: rs1042229
rs1042229
7 0.790 0.280 19 51746419 missense variant A/C;G snv 0.32; 0.13 0.010 1.000 1 2011 2011
dbSNP: rs10434
rs10434
17 0.701 0.480 6 43785475 3 prime UTR variant A/G snv 0.59 0.010 1.000 1 2009 2009
dbSNP: rs1044432
rs1044432
2 0.925 0.080 11 13388251 3 prime UTR variant A/T snv 0.16 0.010 1.000 1 2019 2019