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: rs1934953
rs1934953
2 1.000 0.040 10 95037713 intron variant C/A;T snv 0.010 1.000 1 2017 2017
dbSNP: rs7909236
rs7909236
2 1.000 0.040 10 95069673 upstream gene variant G/T snv 0.18 0.010 1.000 1 2017 2017