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: rs12086634
rs12086634
6 0.827 0.280 1 209706914 intron variant T/G snv 0.21 0.20 0.040 1.000 4 2011 2017
dbSNP: rs846910
rs846910
6 0.882 0.160 1 209701909 intron variant A/G snv 0.95 0.020 1.000 2 2011 2017
dbSNP: rs1000283
rs1000283
2 0.925 0.080 1 209721316 intron variant G/A snv 0.18 0.010 1.000 1 2011 2011
dbSNP: rs45487298
rs45487298
3 0.882 0.120 1 209706871 intron variant -/A delins 0.010 1.000 1 2019 2019
dbSNP: rs846906
rs846906
1 1.000 0.040 1 209714373 intron variant T/A;C snv 0.010 1.000 1 2015 2015