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: rs4721442
rs4721442
2 7 15466382 intron variant T/G snv 0.20 0.700 1.000 2 2019 2019
dbSNP: rs55905169
rs55905169
2 7 15466904 intron variant G/C snv 0.19 0.700 1.000 1 2018 2018