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: rs4684242
rs4684242
4 3 14853598 intron variant G/C snv 0.20 0.700 1.000 2 2018 2018
dbSNP: rs11128722
rs11128722
2 3 14916619 intron variant G/A snv 0.48 0.700 1.000 1 2016 2016
dbSNP: rs12630213
rs12630213
4 3 14912904 intron variant C/T snv 0.68 0.700 1.000 1 2017 2017
dbSNP: rs12635574
rs12635574
1 3 14913042 intron variant A/C snv 0.74 0.700 1.000 1 2019 2019
dbSNP: rs34991912
rs34991912
2 1.000 0.040 3 14884844 intron variant T/A;C snv 0.700 1.000 1 2019 2019
dbSNP: rs78793397
rs78793397
3 3 14905917 intron variant A/G snv 2.7E-02 0.700 1.000 1 2018 2018