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: rs1555738837
rs1555738837
1 1.000 19 35746418 coding sequence variant G/-;GG delins 0.700 0
dbSNP: rs1555738906
rs1555738906
1 1.000 19 35746735 missense variant T/G snv 0.700 0