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: rs10415849
rs10415849
4 19 19394278 intron variant C/T snv 0.12 0.700 1.000 1 2012 2012
dbSNP: rs16996119
rs16996119
2 19 19501816 intron variant G/A;T snv 0.700 1.000 1 2012 2012
dbSNP: rs3794991
rs3794991
5 1.000 0.080 19 19499787 intron variant C/G;T snv 7.4E-02 0.700 1.000 1 2012 2012
dbSNP: rs4808199
rs4808199
5 1.000 0.040 19 19434290 intron variant G/A;T snv 0.19 0.700 1.000 1 2012 2012