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: rs10011796
rs10011796
ABCG2
4 0.882 0.160 4 88169725 intron variant T/C;G snv 0.010 1.000 1 2017 2017
dbSNP: rs11942223
rs11942223
SLC2A9
4 0.882 0.160 4 9961141 intron variant T/C snv 0.28 0.010 < 0.001 1 2017 2017
dbSNP: rs2231142
rs2231142
ABCG2
56 0.583 0.680 4 88131171 missense variant G/C;T snv 4.0E-06; 0.12 0.010 1.000 1 2017 2017