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: rs13191362
rs13191362
3 6 162612318 intron variant A/G snv 8.7E-02 0.700 1.000 6 2015 2019
dbSNP: rs36007635
rs36007635
1 6 162588303 intron variant G/A snv 0.10 0.700 1.000 1 2019 2019