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: rs13238203
rs13238203
1 7 72664689 intron variant C/T snv 1.8E-02 0.800 1.000 2 2010 2018
dbSNP: rs34881399
rs34881399
1 7 72769162 non coding transcript exon variant T/C snv 1.7E-02 0.700 1.000 1 2018 2018