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: rs1537370
rs1537370
2 1.000 9 22084311 intron variant C/T snv 0.55 0.800 1.000 3 2011 2013
dbSNP: rs1333049
rs1333049
60 0.614 0.520 9 22125504 intron variant G/C snv 0.41 0.800 1.000 2 2011 2013
dbSNP: rs10757278
rs10757278
44 0.620 0.520 9 22124478 intron variant A/G snv 0.40 0.700 1.000 3 2011 2013
dbSNP: rs2891168
rs2891168
5 0.851 0.160 9 22098620 intron variant A/G snv 0.40 0.700 1.000 3 2011 2013
dbSNP: rs1004638
rs1004638
3 1.000 0.040 9 22115590 intron variant A/C;T snv 0.700 1.000 2 2011 2013
dbSNP: rs10116277
rs10116277
8 0.827 0.160 9 22081398 intron variant G/T snv 0.62 0.700 1.000 2 2011 2013
dbSNP: rs10511701
rs10511701
2 9 22112600 intron variant T/A;C snv 0.700 1.000 2 2011 2013
dbSNP: rs10733376
rs10733376
3 1.000 0.080 9 22114470 intron variant G/C snv 0.64 0.700 1.000 2 2011 2013
dbSNP: rs10738607
rs10738607
4 0.925 0.080 9 22088095 intron variant A/G snv 0.42 0.700 1.000 2 2011 2013
dbSNP: rs10738609
rs10738609
3 1.000 0.040 9 22114496 intron variant A/C;G;T snv 0.700 1.000 2 2011 2013
dbSNP: rs10738610
rs10738610
5 0.882 0.120 9 22123767 intron variant A/C;T snv 0.700 1.000 2 2011 2013
dbSNP: rs10757269
rs10757269
4 1.000 0.040 9 22072265 intron variant A/C;G snv 0.700 1.000 2 2011 2013
dbSNP: rs10757272
rs10757272
6 0.851 0.160 9 22088261 intron variant C/T snv 0.41 0.700 1.000 2 2011 2013
dbSNP: rs10757274
rs10757274
22 0.701 0.320 9 22096056 intron variant A/G snv 0.41 0.700 1.000 2 2013 2013
dbSNP: rs10811647
rs10811647
3 1.000 0.040 9 22065003 intron variant C/G;T snv 0.700 1.000 2 2011 2013
dbSNP: rs10811650
rs10811650
5 0.882 0.200 9 22067594 intron variant A/G snv 0.37 0.700 1.000 2 2011 2013
dbSNP: rs10811651
rs10811651
2 1.000 0.040 9 22067831 intron variant G/A;C snv 0.700 1.000 2 2011 2013
dbSNP: rs10965224
rs10965224
2 1.000 0.040 9 22067277 intron variant T/A snv 0.64 0.700 1.000 2 2011 2013
dbSNP: rs1333039
rs1333039
2 1.000 0.040 9 22065658 splice region variant G/A;C;T snv 0.700 1.000 2 2011 2013
dbSNP: rs1333042
rs1333042
7 0.827 0.120 9 22103814 intron variant A/G snv 0.63 0.700 1.000 2 2011 2013
dbSNP: rs1333043
rs1333043
2 9 22106732 intron variant T/A snv 0.64 0.700 1.000 2 2011 2013
dbSNP: rs1333046
rs1333046
4 0.925 0.080 9 22124124 intron variant T/A snv 0.43 0.700 1.000 2 2011 2013
dbSNP: rs1333047
rs1333047
9 0.790 0.240 9 22124505 intron variant A/T snv 0.63 0.700 1.000 2 2011 2013
dbSNP: rs1333048
rs1333048
24 0.683 0.320 9 22125348 intron variant A/C snv 0.44 0.700 1.000 2 2011 2013
dbSNP: rs1412834
rs1412834
11 0.790 0.080 9 22110132 intron variant T/C snv 0.64 0.700 1.000 2 2011 2013