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: rs10864294
rs10864294
1 1.000 0.040 1 7333260 intron variant C/T snv 0.19 0.010 1.000 1 2013 2013
dbSNP: rs2301462
rs2301462
1 1.000 0.040 1 7332534 intron variant C/T snv 0.51 0.010 1.000 1 2013 2013