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: rs1168029
rs1168029
1 1 62503731 intron variant G/A;C snv 0.800 1.000 1 2012 2012
dbSNP: rs10889353
rs10889353
5 1 62652525 intron variant A/C;T snv 0.700 1.000 1 2009 2009
dbSNP: rs1167998
rs1167998
6 1 62465961 intron variant C/A snv 0.57 0.700 1.000 1 2009 2009
dbSNP: rs1168041
rs1168041
2 1 62494579 non coding transcript exon variant T/C snv 0.61 0.700 1.000 1 2016 2016