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: rs8170
rs8170
3 0.724 0.160 19 17278895 synonymous variant G/A snv 0.15 0.18 0.750 0.833 2 2010 2014
dbSNP: rs8100241
rs8100241
1 0.827 0.120 19 17282085 missense variant G/A snv 0.47 0.47 0.700 1.000 2 2010 2012
dbSNP: rs10402468
rs10402468
1 1.000 0.080 19 17273194 intron variant C/A snv 0.16 0.700 1.000 1 2010 2010
dbSNP: rs10406920
rs10406920
1 1.000 0.080 19 17278839 splice region variant C/T snv 0.15 0.18 0.700 1.000 1 2010 2010
dbSNP: rs10415471
rs10415471
1 1.000 0.080 19 17250255 synonymous variant C/A;G;T snv 4.1E-06; 0.16 0.700 1.000 1 2010 2010
dbSNP: rs10416654
rs10416654
1 1.000 0.080 19 17274367 intron variant T/C snv 0.17 0.700 1.000 1 2010 2010
dbSNP: rs10418154
rs10418154
1 1.000 0.080 19 17275197 intron variant A/G snv 0.18 0.700 1.000 1 2010 2010
dbSNP: rs10418362
rs10418362
1 1.000 0.080 19 17275298 intron variant A/T snv 0.18 0.700 1.000 1 2010 2010
dbSNP: rs10419397
rs10419397
1 1.000 0.080 19 17280519 intron variant G/A;T snv 0.700 1.000 1 2010 2010
dbSNP: rs10420922
rs10420922
1 1.000 0.080 19 17271696 intron variant A/T snv 0.42 0.50 0.700 1.000 1 2010 2010
dbSNP: rs10424178
rs10424178
1 1.000 0.080 19 17268749 splice region variant C/T snv 0.17 0.23 0.700 1.000 1 2010 2010
dbSNP: rs10426697
rs10426697
1 1.000 0.080 19 17278347 intron variant C/T snv 0.19 0.700 1.000 1 2010 2010
dbSNP: rs11291512
rs11291512
1 1.000 0.080 19 17274572 intron variant AA/-;A;AAA delins 0.43 0.700 1.000 1 2010 2010
dbSNP: rs11667618
rs11667618
1 1.000 0.080 19 17279669 intron variant C/T snv 0.33 0.700 1.000 1 2010 2010
dbSNP: rs11667661
rs11667661
1 1.000 0.080 19 17279770 intron variant C/T snv 0.33 0.700 1.000 1 2010 2010
dbSNP: rs12104352
rs12104352
1 1.000 0.080 19 17266139 intron variant G/T snv 0.35 0.700 1.000 1 2010 2010
dbSNP: rs12980812
rs12980812
1 1.000 0.080 19 17266749 intron variant C/G;T snv 0.23 0.700 1.000 1 2010 2010
dbSNP: rs12982178
rs12982178
1 1.000 0.080 19 17260759 intron variant T/C snv 0.17 0.700 1.000 1 2010 2010
dbSNP: rs34084277
rs34084277
1 1.000 0.080 19 17276367 intron variant A/G snv 0.14 0.17 0.700 1.000 1 2010 2010
dbSNP: rs35256297
rs35256297
1 1.000 0.080 19 17266140 intron variant TT/-;T;TTT;TTTT delins 0.13 0.700 1.000 1 2010 2010
dbSNP: rs35552009
rs35552009
1 1.000 0.080 19 17275299 intron variant T/-;TT;TTT delins 0.700 1.000 1 2010 2010
dbSNP: rs35604430
rs35604430
1 1.000 0.080 19 17272181 intron variant A/G;T snv 0.700 1.000 1 2010 2010
dbSNP: rs35686037
rs35686037
1 1.000 0.080 19 17248726 intron variant C/T snv 0.15 0.700 1.000 1 2010 2010
dbSNP: rs3745185
rs3745185
1 1.000 0.080 19 17273458 intron variant G/A snv 0.36 0.700 1.000 1 2010 2010
dbSNP: rs3837926
rs3837926
1 1.000 0.080 19 17274571 splice region variant T/A snv 0.18 0.700 1.000 1 2010 2010