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: rs12722725
rs12722725
1 1 112716059 non coding transcript exon variant T/C snv 8.9E-02 0.700 1.000 3 2019 2019
dbSNP: rs12736457
rs12736457
1 1 112715671 upstream gene variant C/G snv 8.9E-02 0.700 1.000 1 2019 2019
dbSNP: rs34611728
rs34611728
1 1 112712834 missense variant C/A snv 9.8E-02 8.8E-02 0.700 1.000 1 2019 2019