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: rs9349379
rs9349379
4 0.732 0.200 6 12903725 intron variant A/G snv 0.32 0.820 1.000 4 2011 2019
dbSNP: rs12526453
rs12526453
3 0.827 0.160 6 12927312 intron variant C/G snv 0.27 0.820 1.000 2 2011 2017
dbSNP: rs1332844
rs1332844
1 1.000 0.040 6 12888772 intron variant C/T snv 0.61 0.800 1.000 1 2011 2011