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: rs10483182
rs10483182 		2 22 34739115 intergenic variant G/A snv 1.7E-02 0.700 1.000 1 2016 2016
dbSNP: rs10492494
rs10492494
LOC105370259
1 13 74346049 intron variant C/A snv 0.13 0.700 1.000 1 2015 2015
dbSNP: rs10506418
rs10506418 		2 12 61094991 intergenic variant G/A;T snv 5.5E-02 0.700 1.000 1 2016 2016
dbSNP: rs10520638
rs10520638
AGBL1
2 15 86710303 intron variant C/T snv 5.4E-02 0.700 1.000 1 2016 2016
dbSNP: rs10830963
rs10830963
MTNR1B
27 0.776 0.400 11 92975544 intron variant C/G snv 0.22 0.700 1.000 1 2014 2014
dbSNP: rs11112613
rs11112613 		1 12 105610008 intergenic variant A/G snv 0.14 0.700 1.000 1 2014 2014
dbSNP: rs11187144
rs11187144 		1 10 92710223 downstream gene variant T/C snv 0.39 0.700 1.000 1 2014 2014
dbSNP: rs11627967
rs11627967
NPAS3
2 14 33300706 intron variant G/T snv 5.4E-03 0.700 1.000 1 2016 2016
dbSNP: rs11683087
rs11683087 		1 2 226721890 regulatory region variant G/A snv 0.61 0.700 1.000 1 2015 2015
dbSNP: rs12454712
rs12454712
BCL2
9 0.925 0.120 18 63178651 intron variant T/A;C snv 0.700 1.000 1 2016 2016
dbSNP: rs12583553
rs12583553 		2 13 21758683 intergenic variant A/T snv 2.2E-02 0.700 1.000 1 2016 2016
dbSNP: rs13285079
rs13285079 		1 9 83176735 intergenic variant C/T snv 2.7E-02 0.700 1.000 1 2014 2014
dbSNP: rs13422522
rs13422522
LOC646736
2 2 226146604 intergenic variant C/G snv 0.15 0.700 1.000 1 2016 2016
dbSNP: rs1602084
rs1602084
MFSD8
1 4 127922325 intron variant A/G snv 4.9E-02 0.700 1.000 1 2015 2015
dbSNP: rs17036328
rs17036328
PPARG
3 1.000 0.040 3 12348985 intron variant T/C snv 0.14 0.700 1.000 1 2016 2016
dbSNP: rs174541
rs174541
FADS2
8 1.000 0.080 11 61798436 intron variant T/C snv 0.29 0.700 1.000 1 2013 2013
dbSNP: rs17823642
rs17823642
DMGDH
1 5 79045474 intron variant C/T snv 6.9E-02 0.700 1.000 1 2013 2013
dbSNP: rs1857095
rs1857095 		2 1 79780335 intergenic variant C/T snv 0.88 0.700 1.000 1 2016 2016
dbSNP: rs196701
rs196701
LOC100506851
1 6 79437470 intron variant C/A;T snv 0.700 1.000 1 2015 2015
dbSNP: rs1978648
rs1978648 		1 2 43144403 intergenic variant T/A;C snv 0.700 1.000 1 2015 2015
dbSNP: rs333960
rs333960
LINC01768
2 1 109896858 non coding transcript exon variant C/A;T snv 0.700 1.000 1 2012 2012
dbSNP: rs4078023
rs4078023 		2 16 20308765 downstream gene variant G/A;T snv 0.700 1.000 1 2016 2016
dbSNP: rs478093
rs478093
PHGDH ; LOC105378937
3 1.000 0.040 1 119712503 5 prime UTR variant A/G snv 0.73 0.700 1.000 1 2013 2013
dbSNP: rs4887140
rs4887140
INSYN1 ; INSYN1-AS1
1 15 73754322 intron variant G/A;T snv 0.700 1.000 1 2015 2015
dbSNP: rs499368
rs499368
SLC6A12
1 12 211754 intron variant T/A;C snv 0.700 1.000 1 2013 2013