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: rs10226308
rs10226308
2 7 37898820 intron variant A/C;G snv 0.700 1.000 1 2012 2012
dbSNP: rs1124268
rs1124268
1 7 37945408 intron variant A/G;T snv 0.700 1.000 1 2018 2018