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: rs1007175
rs1007175
TULP3P1 ; LINC00359
1 1.000 0.040 13 96960285 intron variant C/T snv 0.52 0.700 1.000 1 2019 2019
dbSNP: rs12945036
rs12945036
RPH3AL
1 1.000 0.040 17 230930 intron variant C/G snv 0.52 0.700 1.000 1 2019 2019
dbSNP: rs200288366
rs200288366
PRH1 ; PRR4 ; TAS2R14 ; TAS2R43 ; PRH1-PRR4 ; PRH1-TAS2R14
1 1.000 0.040 12 11092003 missense variant T/C snv 0.700 1.000 1 2019 2019
dbSNP: rs2234671
rs2234671
CXCR1
7 0.807 0.240 2 218164385 missense variant C/G snv 9.1E-02 0.11 0.700 1.000 1 2019 2019
dbSNP: rs4899973
rs4899973
FOXN3
1 1.000 0.040 14 89272011 intron variant T/C snv 0.37 0.700 1.000 1 2019 2019
dbSNP: rs55652507
rs55652507 		1 1.000 0.040 5 155502654 intergenic variant A/C snv 0.34 0.700 1.000 1 2019 2019
dbSNP: rs79642714
rs79642714
FAM8A1
1 1.000 0.040 6 17605974 missense variant G/A snv 4.2E-05 4.9E-03 0.700 1.000 1 2019 2019
dbSNP: rs9578751
rs9578751
PARP4 ; TPTE2P6
1 1.000 0.040 13 24500352 missense variant C/T snv 8.9E-02 1.0E-01 0.700 1.000 1 2019 2019