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: rs2984613
rs2984613
1 1 156227589 intron variant C/T snv 0.32 0.800 1.000 1 2014 2014
dbSNP: rs3001789
rs3001789
1 1 156227823 intron variant T/G snv 0.37 0.700 1.000 1 2014 2014
dbSNP: rs6427307
rs6427307
1 1 156220292 intron variant A/G;T snv 0.700 1.000 1 2014 2014
dbSNP: rs7534434
rs7534434
1 1 156216824 intron variant A/G;T snv 0.700 1.000 1 2014 2014
dbSNP: rs887953
rs887953
1 1 156221358 intron variant T/C snv 0.36 0.700 1.000 1 2014 2014