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: rs11575934
rs11575934
IL12RB1
4 0.882 0.040 19 18075808 missense variant T/C snv 0.28 0.25 0.010 1.000 1 2016 2016
dbSNP: rs1359569422
rs1359569422
KIDINS220
1 1.000 0.040 2 8803093 missense variant C/T snv 4.0E-06 0.010 1.000 1 2016 2016
dbSNP: rs4804803
rs4804803
CD209
15 0.732 0.360 19 7747847 upstream gene variant A/G snv 0.26 0.010 1.000 1 2019 2019
dbSNP: rs7975232
rs7975232
VDR
56 0.576 0.760 12 47845054 intron variant C/A snv 0.51 0.55 0.010 1.000 1 2019 2019
dbSNP: rs995043070
rs995043070
KIDINS220
1 1.000 0.040 2 8785880 missense variant G/C snv 0.010 1.000 1 2016 2016