Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4434553
TFR2
1.000 0.040 7 100642568 intron variant A/G snv 0.40 3
rs767057
MAPT ; LOC105371800
0.925 0.120 17 45921456 intron variant A/G snv 0.14 3
rs1052553
MAPT
0.827 0.200 17 45996523 synonymous variant A/G snv 0.14 0.15 2
rs17334797
LINC02210-CRHR1
1.000 0.040 17 45748546 intron variant A/G snv 0.15 2
rs17574361
KANSL1
1.000 0.040 17 46030836 3 prime UTR variant A/G snv 0.14 2
rs1799990
PRNP
0.683 0.440 20 4699605 missense variant A/G snv 0.31 0.33 2
rs4538475
BST1
1.000 0.040 4 15736314 intron variant A/G snv 0.24 2
rs62063857
STH ; MAPT
0.882 0.120 17 45999299 missense variant A/G snv 0.14 0.15 2
rs7225002
KANSL1
0.925 0.080 17 46111701 intron variant A/G snv 0.39 2
rs947211
LOC105371702
0.925 0.040 1 205783537 non coding transcript exon variant A/G snv 0.64 2
rs12456492
RIT2
0.882 0.080 18 43093415 intron variant A/G snv 0.33 1
rs1296028 1.000 0.040 8 11841238 downstream gene variant A/G snv 0.20 1
rs1372519
SNCA-AS1 ; SNCA
1.000 0.040 4 89836158 5 prime UTR variant A/G snv 0.77 1
rs1411478
STX6
0.925 0.120 1 180993146 intron variant A/G snv 0.56 1
rs16938508
KCNB2
1.000 0.040 8 72938577 downstream gene variant A/G snv 0.12 1
rs17563965
MAPT
1.000 0.040 17 45913553 intron variant A/G snv 0.14 1
rs1990622 0.742 0.200 7 12244161 downstream gene variant A/G snv 0.52 1
rs2197120
SNCA
1.000 0.040 4 89808451 intron variant A/G snv 0.78 1
rs2572323
SNCA ; LOC105377329
1.000 0.040 4 89713401 intron variant A/G snv 0.75 1
rs356180
SNCA ; LOC105377329
1.000 0.040 4 89706976 intron variant A/G snv 0.77 1
rs3775478
MMRN1
1.000 0.040 4 89921689 intron variant A/G snv 0.14 1
rs3784847
CDH8
1.000 0.040 16 61943545 intron variant A/G snv 9.5E-02 1
rs4925114
RAI1
0.925 0.080 17 17807956 intron variant A/G snv 0.53 1
rs6532197 1.000 0.040 4 89876150 upstream gene variant A/G snv 0.16 1
rs7846412
PIP4P2
1.000 0.040 8 91032300 intron variant A/G snv 0.47 1