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: rs1800562
rs1800562
HFE ; LOC108783645
262 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 0.800 1.000 4 2009 2012
dbSNP: rs7775698
rs7775698
HBS1L
14 1.000 0.080 6 135097497 intron variant C/T snv 6.9E-02 0.800 1.000 4 2009 2013
dbSNP: rs9349205
rs9349205
CCND3
7 6 41957421 intron variant G/A;C snv 0.800 1.000 4 2009 2018
dbSNP: rs9399137
rs9399137
HBS1L
13 0.851 0.320 6 135097880 intron variant T/C snv 0.20 0.800 1.000 3 2009 2018
dbSNP: rs10758658
rs10758658
RCL1
4 9 4856877 intron variant G/A snv 0.15 0.800 1.000 2 2009 2017
dbSNP: rs11970772
rs11970772
CCND3
5 6 41957552 intron variant T/A snv 0.24 0.700 1.000 2 2009 2016
dbSNP: rs172629
rs172629 		2 4 54541595 intergenic variant C/G snv 0.17 0.800 1.000 2 2009 2010
dbSNP: rs2413450
rs2413450
TMPRSS6
6 22 37074184 intron variant T/C snv 0.61 0.800 1.000 2 2009 2017
dbSNP: rs4820268
rs4820268
TMPRSS6
14 0.851 0.160 22 37073551 missense variant G/A;C snv 0.53; 4.0E-06 0.800 1.000 2 2009 2012
dbSNP: rs4895441
rs4895441
LOC105378010
10 0.925 0.080 6 135105435 upstream gene variant A/G snv 0.21 0.800 1.000 2 2009 2012
dbSNP: rs643381
rs643381 		4 6 139518286 intron variant C/A;G snv 0.800 1.000 2 2009 2017
dbSNP: rs7255045
rs7255045
HOOK2
2 19 12821455 intron variant G/A snv 0.37 0.800 1.000 2 2009 2017
dbSNP: rs9374080
rs9374080
CCDC162P
2 6 109295217 intron variant T/C snv 0.40 0.800 1.000 2 2009 2017
dbSNP: rs9402686
rs9402686
LOC105378010
5 6 135106679 upstream gene variant G/A snv 0.20 0.700 1.000 2 2009 2019
dbSNP: rs9859260
rs9859260
TFRC
2 3 196073676 intron variant C/A;T snv 0.800 1.000 2 2009 2017
dbSNP: rs11239550
rs11239550
MARCHF8
3 10 45529281 intron variant A/G snv 0.31 0.800 1.000 1 2009 2009
dbSNP: rs12718597
rs12718597
IKZF1
2 7 50360730 intron variant C/A;T snv 0.800 1.000 1 2009 2009
dbSNP: rs131794
rs131794
ODF3B
2 22 50533323 upstream gene variant A/C;G;T snv 0.800 1.000 1 2009 2009
dbSNP: rs1408272
rs1408272
SLC17A3
4 6 25842723 intron variant T/G snv 4.0E-02 0.700 1.000 1 2009 2009
dbSNP: rs2540917
rs2540917
MIR4432HG
3 2 60381624 intron variant T/C snv 0.29 0.800 1.000 1 2009 2009
dbSNP: rs4466998
rs4466998
FNTB ; MAX ; CHURC1-FNTB
2 14 65008822 intron variant C/A;G snv 0.800 1.000 1 2009 2009
dbSNP: rs7189020
rs7189020
FAM234A
2 16 254804 intron variant A/T snv 0.55 0.800 1.000 1 2009 2009
dbSNP: rs7786877
rs7786877 		3 7 100616392 downstream gene variant A/G snv 0.22 0.800 1.000 1 2009 2009
dbSNP: rs9609565
rs9609565 		3 22 32471541 upstream gene variant G/A snv 0.24 0.700 1.000 1 2009 2009
dbSNP: rs855791
rs855791
TMPRSS6
38 0.701 0.400 22 37066896 missense variant A/G;T snv 0.57; 4.0E-06 0.800 1.000 7 2010 2019