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: rs712048
rs712048
1 17 35999179 intron variant C/A snv 0.35 0.700 1.000 2 2018 2018
dbSNP: rs16971802
rs16971802
1 17 35984351 missense variant T/C;G snv 4.4E-02 0.700 1.000 1 2018 2018
dbSNP: rs72830000
rs72830000
1 17 35985545 5 prime UTR variant G/A snv 4.9E-02 0.700 1.000 1 2018 2018
dbSNP: rs854624
rs854624
1 17 36000884 intron variant T/G snv 0.23 0.700 1.000 1 2018 2018
dbSNP: rs9892586
rs9892586
1 17 35986879 5 prime UTR variant A/G snv 6.0E-02 0.700 1.000 1 2018 2018
dbSNP: rs9903158
rs9903158
1 17 35985301 5 prime UTR variant T/A;C snv 0.700 1.000 1 2018 2018