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: rs10958476
rs10958476
2 8 56183249 intron variant T/C snv 0.16 0.700 1.000 3 2008 2014
dbSNP: rs13273123
rs13273123
2 8 56188232 intron variant A/G snv 0.14 0.700 1.000 2 2009 2015
dbSNP: rs62515430
rs62515430
1 8 56196799 intron variant C/G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs62515432
rs62515432
1 8 56210964 intron variant T/C snv 0.16 0.700 1.000 1 2017 2017
dbSNP: rs71555635
rs71555635
1 8 56201961 intron variant TTTT/-;TT;TTT;TTTTT;TTTTTT;TTTTTTT;TTTTTTTTT;TTTTTTTTTT;TTTTTTTTTTT delins 0.700 1.000 1 2017 2017
dbSNP: rs72656010
rs72656010
3 8 56209656 intron variant T/C snv 0.10 0.700 1.000 1 2019 2019
dbSNP: rs7833986
rs7833986
2 8 56187590 intron variant G/A snv 0.22 0.700 1.000 1 2010 2010