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: rs1564805114
rs1564805114
1 10 71807558 frameshift variant -/CGAT ins 0.700 0
dbSNP: rs762118583
rs762118583
1 10 71791284 missense variant A/C snv 8.0E-06 7.0E-06 0.700 0