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: rs1018148
rs1018148
1 15 48610929 intron variant A/G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs1036477
rs1036477
5 0.882 0.040 15 48622729 intron variant A/G snv 0.24 0.700 1.000 1 2017 2017
dbSNP: rs1678981
rs1678981
1 15 48607900 intron variant C/T snv 7.7E-02 0.700 1.000 1 2017 2017
dbSNP: rs4775769
rs4775769
2 15 48647691 intron variant T/G snv 0.93 0.700 1.000 1 2019 2019
dbSNP: rs686861
rs686861
2 15 48592808 intron variant A/G snv 9.1E-02 0.700 1.000 1 2018 2018