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: rs4924410
rs4924410
2 1.000 0.040 15 40047293 intron variant A/C snv 0.73 0.800 1.000 1 2012 2012
dbSNP: rs8026641
rs8026641
2 1.000 0.040 15 40046660 intron variant G/A snv 0.73 0.700 1.000 1 2012 2012