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: rs1014369151
rs1014369151
1 1.000 13 27623014 missense variant C/T snv 0.700 0
dbSNP: rs587777841
rs587777841
1 1.000 13 27623011 missense variant C/G snv 0.700 0
dbSNP: rs767196650
rs767196650
1 1.000 13 27622987 missense variant G/A snv 4.0E-06 0.700 0