Source: ALL
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: rs10757212
rs10757212
IFNA5 ; LOC107987053
2 0.925 0.120 9 21304804 synonymous variant G/A snv 0.25 0.27 0.010 1.000 1 2019 2019
dbSNP: rs2069705
rs2069705
IFNG ; IFNG-AS1
19 0.695 0.440 12 68161231 intron variant G/A;C snv 0.010 1.000 1 2019 2019
dbSNP: rs2069718
rs2069718
IFNG ; IFNG-AS1
14 0.742 0.320 12 68156382 intron variant A/G;T snv 0.50 0.010 1.000 1 2019 2019
dbSNP: rs3758236
rs3758236
LOC107987053
1 1.000 0.040 9 21307785 upstream gene variant T/A snv 0.22 0.010 1.000 1 2019 2019