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: rs112785404
rs112785404
1 22 40441831 intron variant T/C snv 2.0E-02 0.700 1.000 1 2019 2019
dbSNP: rs112880707
rs112880707
1 22 40488658 intron variant C/T snv 8.0E-02 0.700 1.000 1 2019 2019
dbSNP: rs17001943
rs17001943
1 22 40466609 intron variant A/G snv 8.4E-02 0.700 1.000 1 2019 2019
dbSNP: rs17001977
rs17001977
1 22 40484209 intron variant G/A snv 7.9E-02 0.700 1.000 1 2019 2019
dbSNP: rs199796575
rs199796575
1 22 40569767 intron variant A/C snv 7.5E-02 0.700 1.000 1 2019 2019
dbSNP: rs6001939
rs6001939
1 22 40496790 intron variant C/T snv 0.14 0.700 1.000 1 2018 2018
dbSNP: rs73167082
rs73167082
1 22 40489495 intron variant T/C snv 7.8E-02 0.700 1.000 1 2019 2019