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: rs1640875
rs1640875
GPRC5A
3 0.882 0.080 12 12916590 3 prime UTR variant A/T snv 0.49 0.700 1.000 1 2018 2018
dbSNP: rs184628474
rs184628474
TTC7B
3 0.882 0.080 14 90719521 intron variant G/A snv 2.9E-02 0.700 1.000 1 2018 2018
dbSNP: rs186133190
rs186133190
WDPCP
3 0.882 0.080 2 63550724 intron variant T/C snv 4.9E-04 0.700 1.000 1 2015 2015
dbSNP: rs2005974
rs2005974
PLA2G6
3 0.882 0.080 22 38141105 non coding transcript exon variant G/A snv 0.49 0.700 1.000 1 2018 2018
dbSNP: rs2111398
rs2111398 		3 0.882 0.080 12 12922268 downstream gene variant A/G snv 0.49 0.700 1.000 1 2015 2015
dbSNP: rs222016
rs222016
GC
3 0.882 0.120 4 71769258 intron variant G/A snv 0.72 0.010 1.000 1 2013 2013
dbSNP: rs2290419
rs2290419
LOC338694
3 0.882 0.080 11 69152181 intron variant A/G snv 4.6E-02 0.700 1.000 1 2015 2015
dbSNP: rs2357176
rs2357176
SYNE2
3 0.882 0.080 14 63942595 intron variant G/A snv 0.68 0.700 1.000 1 2018 2018
dbSNP: rs267600971
rs267600971
CYP21A2 ; DXO ; STK19
3 0.882 0.080 6 31972346 missense variant G/A snv 0.700 1.000 1 2016 2016
dbSNP: rs2695237
rs2695237 		3 0.882 0.080 1 226415934 upstream gene variant T/A;C snv 0.700 1.000 1 2018 2018
dbSNP: rs416981
rs416981
MX2
3 0.882 0.080 21 41373487 intron variant G/A snv 0.48 0.700 1.000 1 2018 2018
dbSNP: rs45575338
rs45575338
TASOR2
3 0.882 0.080 10 5742188 missense variant A/C;G snv 0.19 0.700 1.000 1 2018 2018
dbSNP: rs4670813
rs4670813
CYP1B1 ; CYP1B1-AS1
3 0.882 0.080 2 38090568 intron variant G/A snv 0.40 0.700 1.000 1 2018 2018
dbSNP: rs4731207
rs4731207
GPR37
3 0.882 0.080 7 124756591 intron variant G/A snv 0.47 0.700 1.000 1 2015 2015
dbSNP: rs4731742
rs4731742
LINC-PINT
3 0.882 0.080 7 131070053 intron variant G/A;C snv 0.700 1.000 1 2015 2015
dbSNP: rs55875066
rs55875066
HDAC4
3 0.882 0.080 2 239154306 intron variant C/T snv 6.6E-02 0.700 1.000 1 2018 2018
dbSNP: rs600951
rs600951
DOCK8
3 0.882 0.080 9 224742 intron variant A/G snv 0.61 0.700 1.000 1 2018 2018
dbSNP: rs7041168
rs7041168 		3 0.882 0.080 9 107936435 intergenic variant G/A;T snv 0.700 1.000 1 2015 2015
dbSNP: rs72704658
rs72704658
ARNT
3 0.882 0.080 1 150860534 intron variant T/C snv 0.33 0.700 1.000 1 2018 2018
dbSNP: rs73008229
rs73008229
ATM ; C11orf65
3 0.882 0.080 11 108316962 intron variant G/A snv 0.11 0.700 1.000 1 2018 2018
dbSNP: rs75691080
rs75691080 		3 0.882 0.080 20 63638397 downstream gene variant C/T snv 9.1E-02 0.700 1.000 1 2015 2015
dbSNP: rs758389471
rs758389471
CDKN2A
3 0.882 0.080 9 21971160 missense variant C/G;T snv 4.7E-06; 4.7E-06 0.010 1.000 1 2003 2003
dbSNP: rs910873
rs910873
PIGU
3 0.882 0.160 20 34583968 intron variant G/A;C snv 0.010 < 0.001 1 2009 2009
dbSNP: rs1636744
rs1636744
AHR
4 0.851 0.080 7 16944656 intron variant C/T snv 0.31 0.700 1.000 2 2015 2018
dbSNP: rs498136
rs498136 		4 0.851 0.080 11 69552350 intergenic variant A/C snv 0.68 0.700 1.000 2 2015 2018