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: rs7775698
rs7775698
14 1.000 0.080 6 135097497 intron variant C/T snv 6.9E-02 0.800 1.000 2 2010 2012
dbSNP: rs1331309
rs1331309
2 6 135085040 intron variant T/G snv 0.19 0.700 1.000 1 2018 2018
dbSNP: rs7776054
rs7776054
13 6 135097778 intron variant A/G snv 0.24 0.700 1.000 1 2017 2017
dbSNP: rs9376090
rs9376090
7 6 135090090 intron variant T/C snv 0.19 0.700 1.000 1 2016 2016