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: rs11729441
rs11729441
1 4 183869148 intron variant A/G snv 0.38 0.700 1.000 1 2018 2018
dbSNP: rs6815422
rs6815422
1 4 183902478 intron variant C/T snv 0.51 0.700 1.000 1 2018 2018