Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12507628 4 72779634 regulatory region variant G/A snv 0.13 1
rs1851024 4 71842104 intergenic variant G/A snv 0.93 1
rs2168889 4 74357994 intergenic variant A/G snv 4.7E-02 1
rs2731672
GRK6
5 177415473 intron variant T/C snv 0.66 6
rs13175840 1.000 0.080 5 133861647 regulatory region variant A/G snv 0.25 2
rs6898559
ALDH7A1
1.000 0.080 5 126557237 intron variant G/A snv 0.66 2
rs74910095 1.000 0.080 5 63545132 intergenic variant T/A snv 3.7E-02 2
rs9349379
PHACTR1
0.732 0.200 6 12903725 intron variant A/G snv 0.32 19
rs2026458
PHACTR1
0.882 0.080 6 12825642 intron variant C/T snv 0.34 6
rs16879003
ATXN1
1.000 0.080 6 16745008 intron variant T/C;G snv 2
rs3798722
ELOVL2
6 11040190 intron variant A/G snv 0.39 2
rs59490629
PDSS2
1.000 0.080 6 107256268 intron variant G/A snv 8.5E-02 2
rs9384331
LOC105378054
1.000 0.080 6 150279905 intergenic variant T/C snv 0.12 2
rs10807323
PHACTR1
6 12794799 intron variant G/A snv 0.34 1
rs4711863
PHACTR1
6 12915185 intron variant G/C snv 0.29 1
rs113805659
MAGI2
1.000 0.080 7 78663475 intron variant G/C snv 6.1E-02 2
rs11509197 1.000 0.080 7 118641356 intergenic variant C/T snv 0.38 2
rs117854110 1.000 0.080 7 105603002 upstream gene variant C/A;T snv 2
rs17214144
OSBPL3
1.000 0.080 7 24846128 intron variant T/C snv 0.20 2
rs4272321
PTPRN2
1.000 0.080 7 158159143 intron variant A/G snv 4.6E-04 2
rs7804216
ACTR3C
1.000 0.080 7 149941248 intergenic variant C/G snv 0.24 2
rs91
LOC107986777
1.000 0.080 7 24409992 intron variant T/C snv 0.41 2
rs9641609 1.000 0.080 7 118657790 regulatory region variant A/G snv 0.38 2
rs4841132
LOC157273
8 9326086 non coding transcript exon variant A/G snv 0.89 14
rs12678919 0.882 0.080 8 19986711 intergenic variant A/G snv 1.0E-01 10