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: rs12201899
rs12201899
1 6 45330467 intron variant C/A;T snv 0.700 1.000 1 2018 2018
dbSNP: rs17423748
rs17423748
1 6 44976245 intron variant T/C snv 0.21 0.700 1.000 1 2018 2018
dbSNP: rs184065563
rs184065563
1 6 45176487 intron variant G/A;C;T snv 0.700 1.000 1 2018 2018
dbSNP: rs56283067
rs56283067
1 6 45132593 intron variant T/C snv 0.22 0.700 1.000 1 2018 2018
dbSNP: rs62400317
rs62400317
1 6 45317186 intron variant C/A;T snv 0.700 1.000 1 2018 2018