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: rs3103267
rs3103267
2 2 232123872 intron variant A/C snv 0.72 0.700 1.000 2 2013 2019
dbSNP: rs3116168
rs3116168
1 2 232125121 intron variant T/C;G snv 0.700 1.000 2 2019 2019
dbSNP: rs6717918
rs6717918
2 2 232290400 intron variant T/C snv 0.42 0.700 1.000 2 2009 2019
dbSNP: rs6728302
rs6728302
1 2 232189251 intron variant A/G snv 7.6E-02 0.700 1.000 2 2015 2019
dbSNP: rs7571816
rs7571816
2 2 232212354 intron variant A/G snv 7.4E-02 0.700 1.000 2 2010 2019
dbSNP: rs11677466
rs11677466
1 2 232117547 intron variant A/T snv 5.7E-02 0.700 1.000 1 2014 2014
dbSNP: rs1249260
rs1249260
1 2 232181472 intron variant C/T snv 6.6E-02 0.700 1.000 1 2019 2019
dbSNP: rs2343240
rs2343240
1 2 232222773 intron variant T/C;G snv 0.700 1.000 1 2019 2019
dbSNP: rs7574893
rs7574893
1 2 232225628 intron variant G/T snv 0.93 0.700 1.000 1 2017 2017
dbSNP: rs75877458
rs75877458
1 2 232274083 intron variant T/A snv 1.6E-02 0.700 1.000 1 2019 2019