Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs71413877
LONRF2
2 100308360 intron variant G/A snv 2.6E-02 2
rs7606277
LONRF2
2 100313064 intron variant A/G;T snv 1
rs75152355
LONRF2
2 100319907 intron variant T/C snv 1.4E-02 1
rs11895772
LONRF2
2 100322455 5 prime UTR variant G/A;C snv 1
rs4851300 2 100342342 intergenic variant C/A;T snv 1
rs4851313
CHST10
2 100412540 intron variant G/A snv 0.60 1
rs7590388 2 100425660 non coding transcript exon variant T/G snv 0.58 1
rs9646954 2 100428333 downstream gene variant G/A snv 0.27 1
rs13416322 2 100436121 intergenic variant C/T snv 0.20 1
rs76353274 2 100530994 intergenic variant G/A snv 1.6E-02 1
rs117304774
GRIN2A
1.000 0.040 16 10057377 intron variant G/A snv 8.2E-03 2
rs3112255 2 100700798 intergenic variant C/A snv 0.62 1
rs10175405 2 100703250 regulatory region variant G/T snv 0.33 1
rs1028045 2 100704613 intergenic variant G/A snv 0.38 1
rs7214058
GAS7
1.000 0.040 17 10080017 intron variant T/A;G snv 2
rs7077446
LOC105378458
10 101742008 intergenic variant T/G snv 0.45 1
rs73191547
MSRA
1.000 0.040 8 10175915 intron variant A/T snv 0.28 2
rs749694
LOC105378458
10 101760027 regulatory region variant A/G snv 0.45 2
rs354670
LOC105379102
5 101774594 intergenic variant C/A;T snv 0.71 1
rs2735421
NPM3 ; FGF8
10 101781259 upstream gene variant T/G snv 0.65 2
rs17199964
BANK1
4 101786634 intron variant G/A;C snv 5
rs3740422
OGA
10 101806203 intron variant G/C snv 0.27 1
rs1044258
ARMH3 ; LOC107984029
1.000 0.080 10 101845957 3 prime UTR variant T/C snv 0.26 2
rs13126505
BANK1
1.000 0.040 4 101944147 intron variant G/A snv 4.1E-02 3
rs34592089
BANK1
1.000 0.040 4 102005766 intron variant G/A;T snv 2