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: rs56984562
rs56984562
6 0.827 0.200 1 156137666 missense variant C/A;G;T snv 0.700 1.000 14 2003 2017
dbSNP: rs1553265342
rs1553265342
1 1.000 0.080 1 156134909 missense variant GC/TT mnv 0.700 1.000 11 2000 2015
dbSNP: rs61672878
rs61672878
11 0.776 0.200 1 156136094 missense variant G/A;T snv 0.700 1.000 11 2000 2016
dbSNP: rs267607599
rs267607599
2 0.925 0.120 1 156136422 missense variant A/G;T snv 0.700 1.000 10 2000 2015
dbSNP: rs57520892
rs57520892
8 0.776 0.200 1 156137204 missense variant G/A;C snv 4.1E-05 0.700 1.000 10 1999 2015
dbSNP: rs267607555
rs267607555
6 0.807 0.280 1 156136009 missense variant C/T snv 7.0E-06 0.700 1.000 9 2004 2017
dbSNP: rs397517889
rs397517889
3 0.925 0.120 1 156136093 missense variant C/T snv 7.0E-06 0.700 1.000 9 2003 2014
dbSNP: rs58596362
rs58596362
7 0.827 0.280 1 156138613 splice region variant C/A;T snv 8.1E-06 0.700 1.000 9 2003 2017
dbSNP: rs121912496
rs121912496
3 0.882 0.120 1 156134910 missense variant C/G;T snv 0.700 1.000 8 2008 2015
dbSNP: rs59026483
rs59026483
7 0.827 0.160 1 156134457 missense variant C/T snv 7.0E-06 0.700 1.000 8 2002 2015
dbSNP: rs60458016
rs60458016
5 0.827 0.120 1 156136036 stop gained G/A;T snv 0.700 1.000 8 2000 2014
dbSNP: rs267607571
rs267607571
4 0.882 0.160 1 156134458 missense variant G/A;T snv 0.700 1.000 7 2002 2017
dbSNP: rs60872029
rs60872029
2 0.925 0.120 1 156115010 inframe deletion AAG/- delins 0.700 1.000 7 2002 2014
dbSNP: rs61444459
rs61444459
5 0.851 0.160 1 156137667 missense variant G/A;C snv 0.700 1.000 7 2000 2017
dbSNP: rs61195471
rs61195471
6 0.827 0.160 1 156134496 missense variant G/A snv 0.700 1.000 6 1999 2012
dbSNP: rs150840924
rs150840924
7 0.807 0.240 1 156136359 missense variant C/T snv 8.0E-06 7.0E-06 0.700 1.000 5 2003 2014
dbSNP: rs267607578
rs267607578
3 0.925 0.120 1 156136952 missense variant G/A;C snv 1.4E-05 0.700 1.000 5 2007 2017
dbSNP: rs267607592
rs267607592
2 1.000 0.080 1 156137233 splice donor variant G/A snv 0.700 1.000 5 2005 2014
dbSNP: rs28933091
rs28933091
4 0.882 0.160 1 156134474 missense variant C/A;G snv 0.700 1.000 5 2001 2013
dbSNP: rs58013325
rs58013325
3 1.000 0.080 1 156137144 frameshift variant -/C delins 0.700 1.000 5 2011 2017
dbSNP: rs58932704
rs58932704
8 0.776 0.200 1 156136413 missense variant C/T snv 0.700 1.000 5 1991 2011
dbSNP: rs59332535
rs59332535
5 0.827 0.160 1 156134911 missense variant G/A snv 0.700 1.000 5 2000 2014
dbSNP: rs60682848
rs60682848
11 0.790 0.200 1 156134838 stop gained C/T snv 7.0E-06 0.700 1.000 5 1990 2014
dbSNP: rs60864230
rs60864230
7 0.790 0.280 1 156130658 missense variant G/A;C;T snv 4.0E-06 0.700 1.000 5 2001 2005
dbSNP: rs794728591
rs794728591
2 1.000 0.080 1 156134811 missense variant C/T snv 4.0E-06 7.0E-06 0.700 1.000 5 2013 2018