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: rs1172822
rs1172822
2 1.000 0.040 19 55308477 intron variant C/T snv 0.34 0.800 1.000 3 2009 2013
dbSNP: rs1551562
rs1551562
1 19 55303513 intron variant A/G snv 0.19 0.700 1.000 1 2009 2009