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: rs3807989
rs3807989
2 1.000 0.080 7 116546187 intron variant A/G snv 0.53 0.870 0.875 8 2012 2019
dbSNP: rs11773845
rs11773845
4 0.925 0.120 7 116551247 intron variant C/A snv 0.53 0.710 1.000 4 2017 2018
dbSNP: rs1049334
rs1049334
6 0.851 0.280 7 116560326 3 prime UTR variant G/A;T snv 0.700 1.000 1 2017 2017
dbSNP: rs1997572
rs1997572
1 1.000 0.080 7 116558774 intron variant A/C;G;T snv 0.700 1.000 1 2017 2017