Source: BEFREE ×
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: rs1217691063
rs1217691063
MTHFR
614 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 0.030 1.000 3 2007 2012
dbSNP: rs2544390
rs2544390
LRP2
3 0.925 0.080 2 169348336 intron variant C/T snv 0.45 0.010 1.000 1 2013 2013
dbSNP: rs763059810
rs763059810
CXCR4
41 0.623 0.600 2 136115750 missense variant T/C snv 4.0E-06 0.010 1.000 1 2003 2003
dbSNP: rs1822825
rs1822825
PPARG
2 0.925 0.080 3 12408464 intron variant G/A snv 0.61 0.010 1.000 1 2013 2013
dbSNP: rs4684846
rs4684846
PPARG
3 0.882 0.080 3 12297350 intron variant A/G snv 0.28 0.010 1.000 1 2013 2013
dbSNP: rs2231142
rs2231142
ABCG2
54 0.583 0.680 4 88131171 missense variant G/C;T snv 4.0E-06; 0.12 0.800 1.000 10 2010 2019
dbSNP: rs16890979
rs16890979
SLC2A9
4 0.827 0.200 4 9920543 missense variant C/T snv 0.24 0.29 0.010 1.000 1 2018 2018
dbSNP: rs2054576
rs2054576
ABCG2
1 0.882 0.160 4 88107623 intron variant A/G snv 7.8E-02 0.010 1.000 1 2017 2017
dbSNP: rs4073
rs4073
CXCL8
64 0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46 0.010 1.000 1 2015 2015
dbSNP: rs6837293
rs6837293
PRKG2
2 0.925 0.160 4 81141777 intron variant C/A;T snv 0.010 1.000 1 2009 2009
dbSNP: rs6855911
rs6855911
SLC2A9
3 0.851 0.200 4 9934286 intron variant A/G snv 0.33 0.010 1.000 1 2011 2011
dbSNP: rs72552713
rs72552713
ABCG2
1 0.925 0.040 4 88131805 stop gained G/A snv 4.0E-04 1.2E-04 0.010 1.000 1 2018 2018
dbSNP: rs7688672
rs7688672
PRKG2
2 0.925 0.160 4 81148295 intron variant G/A snv 0.39 0.010 1.000 1 2009 2009
dbSNP: rs33972313
rs33972313
SLC23A1
8 0.790 0.160 5 139379813 missense variant C/A;G;T snv 4.0E-06; 2.7E-02 0.010 1.000 1 2018 2018
dbSNP: rs1800562
rs1800562
HFE ; LOC108783645
230 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 0.010 1.000 1 2017 2017
dbSNP: rs6903956
rs6903956
ADTRP
10 0.763 0.160 6 11774350 intron variant A/G snv 0.65 0.010 1.000 1 2015 2015
dbSNP: rs76863441
rs76863441
PLA2G7
23 0.672 0.440 6 46709361 missense variant C/A snv 4.5E-03 1.3E-03 0.010 1.000 1 2004 2004
dbSNP: rs1209613132
rs1209613132
COL1A2
1 1.000 0.040 7 94404745 missense variant C/T snv 4.0E-06 0.010 1.000 1 2011 2011
dbSNP: rs753397550
rs753397550
COL1A2
1 1.000 0.040 7 94426426 missense variant C/G;T snv 4.6E-06; 9.3E-06 0.010 1.000 1 2011 2011
dbSNP: rs4994
rs4994
ADRB3
65 0.578 0.640 8 37966280 missense variant A/G snv 0.11 9.2E-02 0.040 1.000 4 2007 2013
dbSNP: rs2941484
rs2941484
HNF4G
1 0.882 0.160 8 75566533 3 prime UTR variant C/T snv 0.52 0.010 1.000 1 2017 2017
dbSNP: rs545854
rs545854 		2 0.882 0.160 8 10002570 intron variant G/C snv 0.85 0.010 1.000 1 2019 2019
dbSNP: rs7903456
rs7903456
SHLD2
1 0.882 0.160 10 87159562 intron variant C/T snv 0.69 0.010 1.000 1 2018 2018
dbSNP: rs3825016
rs3825016
SLC22A12
1 0.882 0.160 11 64591814 synonymous variant C/T snv 0.57 0.51 0.020 1.000 2 2015 2018
dbSNP: rs11231825
rs11231825
SLC22A12
3 0.827 0.240 11 64592802 synonymous variant T/C snv 0.57 0.51 0.010 1.000 1 2018 2018