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: rs10278336
rs10278336
2 7 44205764 intron variant A/C;G snv 0.700 1.000 1 2012 2012
dbSNP: rs917793
rs917793
1 7 44206254 intron variant A/T snv 0.21 0.700 1.000 1 2017 2017