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: rs1000778
rs1000778
3 1.000 0.040 11 61887833 intron variant A/G snv 0.59 0.700 1.000 1 2011 2011
dbSNP: rs174450
rs174450
3 1.000 0.080 11 61874070 intron variant G/T snv 0.44 0.700 1.000 1 2011 2011
dbSNP: rs174455
rs174455
5 1.000 0.080 11 61888645 intron variant G/A;C snv 0.700 1.000 1 2011 2011
dbSNP: rs174456
rs174456
2 11 61888710 intron variant C/A snv 0.59 0.700 1.000 1 2011 2011
dbSNP: rs174464
rs174464
2 11 61890454 intron variant A/G snv 0.59 0.700 1.000 1 2011 2011
dbSNP: rs174634
rs174634
2 11 61879915 intron variant G/C;T snv 0.700 1.000 1 2011 2011
dbSNP: rs7394871
rs7394871
2 11 61885042 intron variant A/C;T snv 0.700 1.000 1 2011 2011
dbSNP: rs7942717
rs7942717
2 11 61879816 intron variant G/A snv 0.89 0.700 1.000 1 2011 2011