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: rs1527483
rs1527483
2 1.000 0.080 7 80672184 intron variant G/A snv 6.7E-02 0.040 1.000 4 2010 2018
dbSNP: rs1761667
rs1761667
12 0.752 0.320 7 80615623 intron variant G/A snv 0.49 0.030 1.000 3 2015 2017
dbSNP: rs1194197
rs1194197
2 0.925 0.080 7 80546290 intron variant A/G snv 0.52 0.010 1.000 1 2018 2018
dbSNP: rs3211908
rs3211908
1 1.000 0.080 7 80664600 intron variant C/T snv 5.0E-02 0.010 1.000 1 2010 2010
dbSNP: rs3212018
rs3212018
1 1.000 0.080 7 80674385 3 prime UTR variant GCACAAATAAAGCACT/- del 0.11 0.010 1.000 1 2018 2018
dbSNP: rs7755
rs7755
5 0.882 0.200 7 80676955 3 prime UTR variant G/A snv 0.37 0.010 1.000 1 2018 2018
dbSNP: rs7807607
rs7807607
1 1.000 0.080 7 80597569 intron variant C/T snv 0.53 0.010 1.000 1 2018 2018