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: rs34668726
rs34668726
3 1.000 0.040 2 23673031 intron variant C/G snv 0.13 0.700 1.000 1 2018 2018