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: rs11239537
rs11239537
2 10 45487060 intron variant T/C snv 0.33 0.700 1.000 1 2016 2016
dbSNP: rs11239550
rs11239550
3 10 45529281 intron variant A/G snv 0.31 0.700 1.000 1 2017 2017
dbSNP: rs17157825
rs17157825
2 10 45463228 synonymous variant G/A snv 3.7E-02 3.4E-02 0.700 1.000 1 2018 2018
dbSNP: rs2279434
rs2279434
4 10 45459616 intron variant C/T snv 7.1E-02 0.700 1.000 1 2010 2010
dbSNP: rs35993099
rs35993099
2 10 45511519 intron variant T/A snv 6.2E-02 0.700 1.000 1 2016 2016
dbSNP: rs71494799
rs71494799
1 10 45507408 intron variant T/C snv 4.9E-02 0.700 1.000 1 2019 2019
dbSNP: rs77677521
rs77677521
4 10 45457448 3 prime UTR variant C/G snv 1.3E-02 0.700 1.000 1 2016 2016