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: rs1346408
rs1346408
2 3 141353447 intron variant C/T snv 0.55 0.700 1.000 1 2013 2013
dbSNP: rs6440001
rs6440001
1 3 141367130 3 prime UTR variant T/C snv 0.52 0.700 1.000 1 2013 2013
dbSNP: rs6784404
rs6784404
1 3 141354833 intron variant G/A snv 0.54 0.700 1.000 1 2013 2013
dbSNP: rs7613516
rs7613516
1 3 141360467 intron variant T/G snv 0.56 0.700 1.000 1 2013 2013
dbSNP: rs9866391
rs9866391
2 1.000 0.040 3 141357242 intron variant T/C snv 0.41 0.700 1.000 1 2013 2013