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: rs17122844
rs17122844
2 20 34864797 intron variant C/T snv 0.24 0.700 1.000 1 2010 2010
dbSNP: rs2076668
rs2076668
2 20 34849818 intron variant G/A snv 0.34 0.700 1.000 1 2010 2010
dbSNP: rs6088624
rs6088624
2 20 34849049 intron variant T/A;C snv 0.700 1.000 1 2010 2010
dbSNP: rs6119535
rs6119535
2 20 34854335 intron variant A/C;T snv 0.700 1.000 1 2010 2010
dbSNP: rs6120747
rs6120747
2 20 34861966 intron variant T/C snv 0.32 0.700 1.000 1 2010 2010