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: rs3791679
rs3791679
11 0.925 0.120 2 55869757 intron variant A/G snv 0.20 0.700 1.000 7 2008 2019
dbSNP: rs3791675
rs3791675
4 1.000 0.040 2 55884174 intron variant C/T snv 0.20 0.700 1.000 6 2008 2019
dbSNP: rs11899888
rs11899888
2 2 55875609 intron variant A/G snv 0.11 0.700 1.000 1 2017 2017
dbSNP: rs3828239
rs3828239
1 2 55901165 intron variant A/C;T snv 0.700 1.000 1 2017 2017
dbSNP: rs59985551
rs59985551
2 2 55879793 intron variant C/T snv 0.21 0.700 1.000 1 2019 2019