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: rs45507199
rs45507199
3 0.925 0.120 16 2088294 missense variant G/A;C;T snv 0.700 1.000 9 1998 2016
dbSNP: rs45517258
rs45517258
2 0.925 0.120 16 2076141 missense variant C/G;T snv 0.700 1.000 9 1998 2015
dbSNP: rs45516293
rs45516293
2 0.925 0.120 16 2084965 missense variant A/C;G snv 0.700 1.000 4 2001 2013
dbSNP: rs45517308
rs45517308
2 0.925 0.120 16 2081734 stop gained C/A;G;T snv 8.0E-06 0.700 1.000 4 2001 2017
dbSNP: rs137854052
rs137854052
1 1.000 0.120 16 2058765 frameshift variant -/C delins 0.700 1.000 2 2001 2001
dbSNP: rs137854106
rs137854106
1 1.000 0.120 16 2079357 frameshift variant A/- delins 0.700 1.000 2 2001 2001
dbSNP: rs1567533189
rs1567533189
2 0.925 0.160 16 2086283 frameshift variant AAGGACTGCCA/- del 0.700 1.000 1 2019 2019
dbSNP: rs45517115
rs45517115
1 1.000 0.120 16 2055518 stop gained C/T snv 0.700 1.000 1 2002 2002
dbSNP: rs45517201
rs45517201
1 1.000 0.120 16 2070531 missense variant T/C snv 0.700 1.000 1 2008 2008
dbSNP: rs137854218
rs137854218
3 0.925 0.120 16 2088293 inframe insertion CATCAAGCGGCTCCGCCA/-;CATCAAGCGGCTCCGCCACATCAAGCGGCTCCGCCA delins 0.700 0
dbSNP: rs137854329
rs137854329
1 1.000 0.120 16 2085238 frameshift variant -/T delins 0.700 0
dbSNP: rs45460895
rs45460895
1 1.000 0.120 16 2055520 splice donor variant G/A snv 0.700 0
dbSNP: rs45483392
rs45483392
2 0.925 0.120 16 2087897 missense variant C/A;T snv 0.700 0
dbSNP: rs45488500
rs45488500
1 1.000 0.120 16 2054441 splice donor variant G/T snv 0.700 0
dbSNP: rs45517169
rs45517169
2 0.925 0.120 16 2062982 stop gained C/T snv 0.700 0
dbSNP: rs45517382
rs45517382
2 0.925 0.120 16 2086834 missense variant A/G snv 0.700 0
dbSNP: rs1060500931
rs1060500931
2 0.925 0.120 16 2064302 stop gained C/T snv 0.010 1.000 1 2012 2012
dbSNP: rs1114167462
rs1114167462
2 1.000 0.120 16 2062533 stop gained C/T snv 0.010 1.000 1 2012 2012
dbSNP: rs1430119276
rs1430119276
1 1.000 0.120 16 2079096 missense variant G/T snv 7.0E-06 0.010 < 0.001 1 2019 2019
dbSNP: rs1459518095
rs1459518095
1 1.000 0.120 16 2084552 missense variant C/G;T snv 4.2E-06 0.010 1.000 1 2012 2012
dbSNP: rs28934872
rs28934872
5 0.851 0.200 16 2070571 missense variant G/A snv 0.010 1.000 1 2019 2019
dbSNP: rs376285784
rs376285784
2 1.000 0.120 16 2064342 missense variant G/A snv 1.2E-05 2.1E-05 0.010 1.000 1 2011 2011
dbSNP: rs397514914
rs397514914
2 1.000 0.120 16 2071534 missense variant C/T snv 0.010 1.000 1 2017 2017
dbSNP: rs397514916
rs397514916
2 0.925 0.120 16 2083754 missense variant C/G;T snv 0.010 1.000 1 2012 2012
dbSNP: rs397515225
rs397515225
1 1.000 0.120 16 2080366 missense variant G/A;C snv 4.0E-06 0.010 1.000 1 2017 2017