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: rs112233623
rs112233623
5 6 41957260 intron variant C/T snv 7.0E-03 0.700 1.000 2 2016 2017
dbSNP: rs9349205
rs9349205
7 6 41957421 intron variant G/A;C snv 0.700 1.000 2 2017 2019
dbSNP: rs143111788
rs143111788
2 6 41951438 intron variant AGCTACTC/- delins 0.59 0.700 1.000 1 2016 2016
dbSNP: rs3218092
rs3218092
2 6 41938923 intron variant A/G snv 0.18 0.700 1.000 1 2016 2016
dbSNP: rs4554318
rs4554318
4 6 42044421 intron variant C/T snv 0.55 0.700 1.000 1 2019 2019
dbSNP: rs9394841
rs9394841
3 6 41959197 intron variant T/C snv 0.22 0.700 1.000 1 2016 2016