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: rs1152578
rs1152578
1 1.000 0.040 14 64230319 intron variant T/A;C snv 0.700 1.000 1 2019 2019
dbSNP: rs915057
rs915057
1 1.000 0.040 14 64219489 intron variant A/G;T snv 0.700 1.000 1 2018 2018
dbSNP: rs1256049
rs1256049
32 0.645 0.560 14 64257333 synonymous variant C/T snv 6.7E-02 6.3E-02 0.010 1.000 1 2017 2017
dbSNP: rs4986938
rs4986938
35 0.641 0.600 14 64233098 3 prime UTR variant C/T snv 0.31 0.33 0.010 1.000 1 2017 2017