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: rs10504576
rs10504576
1 8 74354444 intron variant A/G snv 0.47 0.700 1.000 1 2007 2007
dbSNP: rs4469448
rs4469448
1 8 74382875 intron variant G/C;T snv 0.700 1.000 1 2007 2007
dbSNP: rs6996971
rs6996971
1 8 74380257 intron variant C/T snv 0.51 0.700 1.000 1 2007 2007