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: rs12903896
rs12903896 		1 15 74760154 downstream gene variant C/T snv 0.43 0.700 1.000 2 2016 2019
dbSNP: rs143593369
rs143593369 		1 7 100711557 downstream gene variant A/G snv 4.8E-03 0.700 1.000 2 2016 2019
dbSNP: rs16929368
rs16929368
CACNA1C
1 12 2414606 intron variant T/A;C snv 0.700 1.000 2 2018 2019
dbSNP: rs3767844
rs3767844
PROX1
1 1 214007378 intron variant A/G snv 0.35 0.700 1.000 2 2016 2019
dbSNP: rs7583880
rs7583880
KLF7
1 2 207134989 intron variant G/A snv 0.65 0.700 1.000 2 2016 2019
dbSNP: rs78415359
rs78415359
CTIF ; LOC105372107
1 18 48680897 intron variant G/A snv 1.9E-02 0.700 1.000 2 2016 2019
dbSNP: rs9549260
rs9549260 		1 13 40679967 intergenic variant C/A snv 0.27 0.700 1.000 2 2016 2019
dbSNP: rs10049413
rs10049413
TRAIP
1 3 49855463 intron variant A/G snv 0.24 0.700 1.000 1 2019 2019
dbSNP: rs1009110
rs1009110
COG1
1 17 73199810 intron variant C/T snv 0.52 0.700 1.000 1 2019 2019
dbSNP: rs10092747
rs10092747
TAF2
1 8 119736926 intron variant C/G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs1011167
rs1011167
SP4
1 7 21489977 intron variant A/C snv 0.33 0.700 1.000 1 2019 2019
dbSNP: rs10137527
rs10137527 		1 14 105134327 intron variant C/T snv 8.3E-02 0.700 1.000 1 2019 2019
dbSNP: rs10191559
rs10191559
UBE2E3
1 2 181075915 intron variant G/A snv 0.76 0.700 1.000 1 2016 2016
dbSNP: rs10205410
rs10205410
SPTBN1
1 2 54572462 intron variant G/T snv 0.31 0.700 1.000 1 2019 2019
dbSNP: rs1021797
rs1021797
ITPR2
1 12 26413499 intron variant A/C snv 4.7E-02 0.700 1.000 1 2019 2019
dbSNP: rs10226458
rs10226458 		1 7 47595969 intergenic variant T/A snv 0.65 0.700 1.000 1 2019 2019
dbSNP: rs10305916
rs10305916
EDNRA
1 4 147536174 intron variant T/G snv 0.21 0.700 1.000 1 2019 2019
dbSNP: rs10421876
rs10421876
SLC7A9
1 19 32871878 upstream gene variant C/T snv 0.36 0.700 1.000 1 2019 2019
dbSNP: rs10423902
rs10423902 		1 19 33273956 intergenic variant G/A;T snv 0.700 1.000 1 2018 2018
dbSNP: rs10430643
rs10430643
RNLS
1 10 88550323 intron variant T/A;C snv 0.45 0.700 1.000 1 2019 2019
dbSNP: rs10483981
rs10483981
FLRT2
1 14 85653458 3 prime UTR variant C/T snv 0.27 0.700 1.000 1 2019 2019
dbSNP: rs10486757
rs10486757
GRB10
1 7 50626161 intron variant G/A snv 8.8E-02 0.700 1.000 1 2019 2019
dbSNP: rs1050338
rs1050338
ZMIZ2
1 7 44768624 3 prime UTR variant G/A snv 0.39 0.700 1.000 1 2016 2016
dbSNP: rs1051130
rs1051130
CCND3
1 6 41936044 missense variant A/C;G;T snv 0.54; 1.6E-05 0.700 1.000 1 2009 2009
dbSNP: rs10517660
rs10517660
PDGFC
1 4 156921244 intron variant A/G snv 0.50 0.700 1.000 1 2019 2019