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: rs2239647
rs2239647
7 0.851 0.080 14 32823537 synonymous variant A/C snv 0.60 0.65 0.700 1.000 4 2018 2019
dbSNP: rs12885221
rs12885221
1 14 32809804 intron variant G/A;C snv 0.700 1.000 3 2018 2019
dbSNP: rs7146202
rs7146202
1 14 32834311 3 prime UTR variant A/G snv 0.46 0.700 1.000 2 2018 2018
dbSNP: rs10133551
rs10133551
1 14 32813026 intron variant T/C snv 0.30 0.700 1.000 1 2018 2018
dbSNP: rs10147849
rs10147849
1 14 32835225 3 prime UTR variant T/C snv 0.46 0.700 1.000 1 2019 2019
dbSNP: rs17522122
rs17522122
5 0.925 0.040 14 32833676 3 prime UTR variant G/T snv 0.41 0.700 1.000 1 2015 2015
dbSNP: rs2007669
rs2007669
1 14 32819801 intron variant A/C;T snv 0.700 1.000 1 2018 2018
dbSNP: rs4261436
rs4261436
3 0.925 0.040 14 32830276 3 prime UTR variant T/C snv 0.43 0.700 1.000 1 2019 2019