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: rs17011903
rs17011903
PLXNA2
2 0.925 0.040 1 208086186 intron variant C/A snv 1.4E-02 0.700 1.000 1 2019 2019
dbSNP: rs17025736
rs17025736
SLC16A4
2 0.925 0.040 1 110388397 intron variant G/A snv 5.0E-02 0.700 1.000 1 2018 2018
dbSNP: rs17093334
rs17093334
LOC105378798
2 0.925 0.040 1 72708223 intron variant G/A;T snv 0.700 1.000 1 2018 2018
dbSNP: rs17130220
rs17130220
PKN2-AS1
2 0.925 0.040 1 87933704 intron variant T/C snv 4.1E-02 0.700 1.000 1 2018 2018
dbSNP: rs1883758
rs1883758
TMEM51
2 0.925 0.040 1 15177155 intron variant C/T snv 0.70 0.700 1.000 1 2018 2018
dbSNP: rs2004962
rs2004962
AK5
2 0.925 0.040 1 77280560 upstream gene variant G/C snv 9.9E-02 0.700 1.000 1 2018 2018
dbSNP: rs2046158
rs2046158
COL24A1
2 0.925 0.040 1 85865087 intron variant C/T snv 0.13 0.700 1.000 1 2018 2018
dbSNP: rs2050691
rs2050691 		2 0.925 0.040 1 211185838 intron variant C/T snv 7.4E-02 0.700 1.000 1 2018 2018
dbSNP: rs214321
rs214321
CAPZB
2 0.925 0.040 1 19366634 intron variant C/A snv 0.45 0.700 1.000 1 2018 2018
dbSNP: rs2273673
rs2273673
PCNX2
2 0.925 0.040 1 233040288 intron variant C/T snv 0.11 0.700 1.000 1 2018 2018
dbSNP: rs2352036
rs2352036
PTGFR ; MGC27382
2 0.925 0.040 1 78324107 intron variant A/G snv 0.97 0.700 1.000 1 2018 2018
dbSNP: rs2576221
rs2576221
ESRRG
2 0.925 0.040 1 216960347 intron variant C/T snv 0.52 0.700 1.000 1 2018 2018
dbSNP: rs267689
rs267689 		2 0.925 0.040 1 29993005 intergenic variant A/C snv 8.5E-02 0.700 1.000 1 2018 2018
dbSNP: rs2774316
rs2774316
GNG4
2 0.925 0.040 1 235590943 intron variant G/C snv 0.34 0.700 1.000 1 2018 2018
dbSNP: rs2797436
rs2797436
RYR2
2 0.925 0.040 1 237700418 synonymous variant T/A;G snv 7.0E-05; 0.99 0.700 1.000 1 2018 2018
dbSNP: rs2802993
rs2802993 		2 0.925 0.040 1 234905572 intron variant C/T snv 0.98 0.700 1.000 1 2018 2018
dbSNP: rs2816992
rs2816992
NR5A2 ; LOC107985244
4 0.925 0.040 1 200100088 intron variant A/G snv 0.39 0.700 1.000 1 2018 2018
dbSNP: rs2818766
rs2818766
ESRRG
2 0.925 0.040 1 216993402 intron variant T/C snv 0.86 0.700 1.000 1 2018 2018
dbSNP: rs285460
rs285460
LRRC52-AS1
2 0.925 0.040 1 165527244 intron variant G/C snv 0.97 0.700 1.000 1 2018 2018
dbSNP: rs3008590
rs3008590 		2 0.925 0.040 1 196031114 intergenic variant C/T snv 0.32 0.700 1.000 1 2018 2018
dbSNP: rs301696
rs301696
SLC9C2
2 0.925 0.040 1 173539646 intron variant T/A;C;G snv 0.700 1.000 1 2018 2018
dbSNP: rs3026947
rs3026947 		2 0.925 0.040 1 159168677 upstream gene variant T/C snv 6.4E-02 0.700 1.000 1 2018 2018
dbSNP: rs33945715
rs33945715 		2 0.925 0.040 1 192704395 intron variant C/T snv 0.11 0.700 1.000 1 2018 2018
dbSNP: rs34216521
rs34216521 		2 0.925 0.040 1 153368173 intergenic variant T/C snv 0.18 0.700 1.000 1 2018 2018
dbSNP: rs3754260
rs3754260
DAB1
2 0.925 0.040 1 57086566 intron variant G/A snv 0.16 0.700 1.000 1 2018 2018