Source: INFERRED ×
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: rs7163848
rs7163848
1 15 82729563 intron variant C/T snv 0.16 0.700 1.000 1 2018 2018
dbSNP: rs8028130
rs8028130
1 15 82734974 intron variant C/T snv 0.17 0.700 1.000 1 2018 2018