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: rs16867574
rs16867574
1 5 38708452 intron variant C/T snv 0.58 0.700 1.000 1 2019 2019
dbSNP: rs4869589
rs4869589
1 5 38707769 intron variant T/A;G snv 0.59 0.700 1.000 1 2019 2019