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: rs10956412
rs10956412
1 1.000 0.040 8 128150251 intron variant A/C;G snv 0.700 1.000 1 2019 2019