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 0.800 1.000 2 2013 2019
dbSNP: rs10054063
rs10054063 		4 5 173965395 downstream gene variant A/T snv 0.26 0.700 1.000 1 2018 2018
dbSNP: rs10087900
rs10087900 		1 8 143221248 downstream gene variant G/A snv 0.37 0.700 1.000 1 2018 2018
dbSNP: rs10091038
rs10091038 		1 8 29502788 intergenic variant A/C snv 0.57 0.700 1.000 1 2018 2018
dbSNP: rs1009360
rs1009360
LINC02245 ; LINC02576 ; LOC107984063
2 2 65048915 intron variant T/C snv 0.51 0.700 1.000 1 2018 2018
dbSNP: rs10096633
rs10096633 		8 1.000 0.040 8 19973410 regulatory region variant C/T snv 0.22 0.800 1.000 4 2011 2019
dbSNP: rs10099160
rs10099160
LPL
2 8 19964304 intron variant T/G snv 0.20 0.700 1.000 1 2012 2012
dbSNP: rs10105606
rs10105606 		2 8 19970337 downstream gene variant C/A snv 0.42 0.700 1.000 1 2019 2019
dbSNP: rs10106652
rs10106652 		3 1.000 0.040 8 20070649 intergenic variant G/A snv 0.29 0.700 1.000 2 2018 2019
dbSNP: rs10107815
rs10107815
MSRA
4 8 10156645 intron variant G/C snv 5.1E-02 0.700 1.000 1 2012 2012
dbSNP: rs1011731
rs1011731
PIGC ; DNM3
4 1 172377408 intron variant G/A snv 0.46 0.700 1.000 1 2017 2017
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: rs10127775
rs10127775
GALNT2
4 1 230160042 intron variant A/G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs10149080
rs10149080
GCH1
2 14 54889676 intron variant C/T snv 4.4E-02 0.700 1.000 1 2012 2012
dbSNP: rs10184004
rs10184004 		5 1.000 0.080 2 164651879 downstream gene variant C/T snv 0.48 0.700 1.000 1 2018 2018
dbSNP: rs10185855
rs10185855
TBC1D8
4 2 101025798 intron variant A/G snv 0.35 0.700 1.000 1 2018 2018
dbSNP: rs10198423
rs10198423 		1 2 85333439 upstream gene variant G/A;C;T snv 0.700 1.000 1 2018 2018
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 0.800 1.000 2 2010 2012
dbSNP: rs10239940
rs10239940
BAZ1B
2 7 73487060 intron variant A/T snv 2.6E-02 0.700 1.000 1 2012 2012
dbSNP: rs1026422
rs1026422 		1 7 50280211 upstream gene variant G/A snv 0.51 0.700 1.000 1 2018 2018
dbSNP: rs10271556
rs10271556
NAMPT
4 7 106258428 intron variant C/T snv 5.6E-02 0.700 1.000 1 2012 2012