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: rs1000879
rs1000879
VIL1
3 2 218439407 intron variant G/A snv 4.1E-02 0.700 1.000 1 2012 2012
dbSNP: rs10019888
rs10019888 		3 4 26061368 regulatory region variant A/G snv 0.17 0.700 1.000 1 2013 2013
dbSNP: rs10096633
rs10096633 		8 1.000 0.040 8 19973410 regulatory region variant C/T snv 0.22 0.700 1.000 1 2012 2012
dbSNP: rs10099160
rs10099160
LPL
2 8 19964304 intron variant T/G snv 0.20 0.700 1.000 1 2012 2012
dbSNP: rs10107815
rs10107815
MSRA
4 8 10156645 intron variant G/C snv 5.1E-02 0.700 1.000 1 2012 2012
dbSNP: rs10120087
rs10120087
ABCA1
2 9 104898869 intron variant C/A;T snv 0.700 1.000 1 2012 2012
dbSNP: rs10120653
rs10120653
RXRA
3 9 134415237 intron variant G/T snv 1.2E-02 0.700 1.000 1 2012 2012
dbSNP: rs10149080
rs10149080
GCH1
2 14 54889676 intron variant C/T snv 4.4E-02 0.700 1.000 1 2012 2012
dbSNP: rs10200587
rs10200587
BMPR2
2 2 202554561 intron variant A/G snv 7.0E-03 0.700 1.000 1 2012 2012
dbSNP: rs10212938
rs10212938
NPY2R ; LOC107986321
2 4 155207180 non coding transcript exon variant T/C snv 2.6E-02 0.700 1.000 1 2012 2012
dbSNP: rs102275
rs102275
TMEM258
18 0.827 0.320 11 61790331 non coding transcript exon variant T/C snv 0.47 0.700 1.000 1 2012 2012
dbSNP: rs10239940
rs10239940
BAZ1B
2 7 73487060 intron variant A/T snv 2.6E-02 0.700 1.000 1 2012 2012
dbSNP: rs10271556
rs10271556
NAMPT
4 7 106258428 intron variant C/T snv 5.6E-02 0.700 1.000 1 2012 2012
dbSNP: rs10305650
rs10305650
ARNT
2 1 150876501 intron variant G/A;C snv 1.3E-02 0.700 1.000 1 2012 2012
dbSNP: rs10305685
rs10305685
ARNT
2 1 150838529 intron variant T/C snv 5.4E-02 0.700 1.000 1 2012 2012
dbSNP: rs1031045
rs1031045
LPL
3 8 19943601 intron variant G/A snv 0.12 0.700 1.000 1 2012 2012
dbSNP: rs103294
rs103294 		7 0.827 0.200 19 54293995 downstream gene variant T/C snv 0.82 0.700 1.000 1 2012 2012
dbSNP: rs10402729
rs10402729
NCAN
4 19 19244291 intron variant T/C snv 3.3E-02 0.700 1.000 1 2012 2012
dbSNP: rs10405178
rs10405178
SLC25A42
2 19 19064943 intron variant T/G snv 2.5E-02 0.700 1.000 1 2012 2012
dbSNP: rs10411413
rs10411413
SUGP2
2 19 19009572 intron variant C/T snv 2.4E-02 0.700 1.000 1 2012 2012
dbSNP: rs10422058
rs10422058
ARMC6
2 19 19047391 intron variant T/A;C snv 0.700 1.000 1 2012 2012
dbSNP: rs10427943
rs10427943
CABIN1
2 22 24131331 intron variant G/T snv 1.2E-02 0.700 1.000 1 2012 2012
dbSNP: rs10478730
rs10478730
EDN1
5 6 12297276 downstream gene variant C/T snv 1.2E-02 0.700 1.000 1 2012 2012
dbSNP: rs1047891
rs1047891
CPS1
34 0.827 0.200 2 210675783 missense variant C/A snv 0.30 0.33 0.700 1.000 1 2013 2013
dbSNP: rs10484766
rs10484766
ARG1 ; MED23
4 6 131578846 intron variant C/T snv 3.3E-02 0.700 1.000 1 2012 2012