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: rs11138902
rs11138902
1 9 69488398 intron variant G/A;T snv 0.700 1.000 4 2017 2019
dbSNP: rs1105307
rs1105307
1 9 69431124 3 prime UTR variant G/A snv 0.32 0.700 1.000 1 2017 2017
dbSNP: rs7033137
rs7033137
1 9 69440242 intron variant C/G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs7049022
rs7049022
1 9 69440259 intron variant A/G snv 0.20 0.700 1.000 1 2019 2019
dbSNP: rs7859472
rs7859472
1 9 69490489 intron variant T/A snv 0.78 0.700 1.000 1 2019 2019
dbSNP: rs4744899
rs4744899
2 1.000 0.040 9 69461631 non coding transcript exon variant A/G snv 0.55 0.700 1.000 1 2019 2019