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: rs2231142
rs2231142
56 0.583 0.680 4 88131171 missense variant G/C;T snv 4.0E-06; 0.12 0.820 1.000 12 2008 2019
dbSNP: rs4148155
rs4148155
5 0.882 0.200 4 88133515 intron variant A/G snv 8.7E-02 0.800 1.000 5 2010 2019
dbSNP: rs10011796
rs10011796
4 0.882 0.160 4 88169725 intron variant T/C;G snv 0.800 1.000 4 2010 2015
dbSNP: rs3114020
rs3114020
5 0.882 0.200 4 88162514 intron variant T/C snv 0.40 0.800 1.000 4 2010 2017
dbSNP: rs1481012
rs1481012
6 0.882 0.200 4 88117930 intron variant A/G snv 8.9E-02 0.800 1.000 3 2010 2013
dbSNP: rs10009618
rs10009618
3 0.925 0.120 4 88172856 intron variant C/T snv 0.58 0.700 1.000 3 2010 2013
dbSNP: rs12505410
rs12505410
3 0.925 0.120 4 88109689 intron variant T/C;G snv 0.700 1.000 3 2010 2013
dbSNP: rs13120400
rs13120400
2 0.925 0.120 4 88112375 intron variant T/C snv 0.21 0.700 1.000 3 2010 2013
dbSNP: rs1481017
rs1481017
4 0.882 0.160 4 88176325 intron variant C/T snv 0.59 0.700 1.000 3 2010 2013
dbSNP: rs17731799
rs17731799
3 0.925 0.120 4 88147303 intron variant G/A;T snv 0.700 1.000 3 2010 2013
dbSNP: rs2054576
rs2054576
4 0.882 0.160 4 88107623 intron variant A/G snv 7.8E-02 0.700 1.000 3 2010 2013
dbSNP: rs2622604
rs2622604
2 0.925 0.120 4 88157772 intron variant T/A;C snv 0.700 1.000 3 2010 2013
dbSNP: rs2622605
rs2622605
3 0.925 0.120 4 88158234 intron variant T/A;C snv 0.40 0.700 1.000 3 2010 2013
dbSNP: rs2622621
rs2622621
6 0.851 0.240 4 88109768 intron variant C/A;G snv 0.700 1.000 3 2010 2013
dbSNP: rs2622624
rs2622624
3 0.925 0.120 4 88148254 intron variant T/C snv 0.41 0.700 1.000 3 2010 2013
dbSNP: rs2622626
rs2622626
3 0.925 0.120 4 88145563 intron variant C/A snv 0.47 0.700 1.000 3 2010 2013
dbSNP: rs3109823
rs3109823
2 0.925 0.120 4 88143450 intron variant C/T snv 0.65 0.700 1.000 3 2010 2013
dbSNP: rs3114018
rs3114018
4 0.882 0.160 4 88143429 intron variant A/C snv 0.48 0.700 1.000 3 2010 2013
dbSNP: rs4148157
rs4148157
3 0.925 0.120 4 88099782 intron variant G/A snv 7.8E-02 0.700 1.000 3 2010 2013
dbSNP: rs11724427
rs11724427
2 0.925 0.120 4 88182020 intron variant A/C;G;T snv 0.700 1.000 2 2010 2013
dbSNP: rs13108900
rs13108900
2 0.925 0.120 4 88195550 intron variant C/G snv 0.84 0.700 1.000 2 2010 2013
dbSNP: rs13137622
rs13137622
2 0.925 0.120 4 88141361 intron variant G/T snv 0.34 0.700 1.000 2 2010 2013
dbSNP: rs2127863
rs2127863
3 0.882 0.160 4 88190316 intron variant T/C snv 0.84 0.700 1.000 2 2010 2013
dbSNP: rs2231148
rs2231148
2 0.925 0.120 4 88107326 intron variant T/A;C snv 0.700 1.000 2 2010 2013
dbSNP: rs2231156
rs2231156
3 0.925 0.120 4 88099275 intron variant C/A snv 0.10 7.8E-02 0.700 1.000 2 2010 2013