Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6590816
ARHGAP42
11 100730902 intron variant G/A snv 0.40 4
rs6969780
HOXA-AS2 ; HOXA3
7 27119517 splice region variant G/A;C snv 4
rs7302981
CERS5
12 50144032 missense variant A/G;T snv 0.69 0.71 4
rs751984
LRRC10B
11 61510774 3 prime UTR variant T/C snv 0.16 4
rs76987554
TARID
6 133759717 intron variant C/T snv 2.9E-02 4
rs8098380
YES1
18 721563 downstream gene variant A/C snv 0.33 4
rs891511
NOS3
7 151007755 intron variant G/A;C snv 4
rs9814480
CACNA1D
3 53556438 intron variant C/T snv 0.14 4
rs1027989
LYN
8 55901862 intron variant G/A;C snv 3
rs1057518797
PKD2
4 88008090 frameshift variant CCCGGGCA/TAGGACG delins 3
rs10745332
CAPZA1
1 112646431 intron variant G/A snv 0.77 3
rs11067763
LOC105370003
12 115760536 intron variant A/G snv 0.16 3
rs11229457
OR5B12
11 58439730 missense variant C/G;T snv 0.21 0.22 3
rs112913898 10 103199143 intergenic variant G/A snv 9.1E-02 3
rs115236533
CDH18
5 19745606 intron variant G/C snv 3.9E-03 3
rs11563582 7 27312031 intergenic variant G/A snv 9.8E-02 3
rs115795127
FRMD3
9 83378986 intron variant T/C snv 3.4E-02 3
rs11977526
LOC102723446
7 45968511 intron variant G/A;T snv 3
rs12046278
CASZ1
1 10739520 intron variant T/C snv 0.36 3
rs12063100 1 188865413 downstream gene variant G/A;T snv 3
rs13143871
GUCY1A1
4 155698052 intron variant T/C snv 0.25 3
rs139293840
RPTOR
17 80556559 intron variant G/A snv 3.3E-04 3
rs186208701
STK3
8 98567888 intron variant T/C snv 3.3E-03 3
rs187821766
STK3
8 98729050 intron variant C/T snv 3.5E-03 3
rs2021783
TNXB
6 32077074 intron variant C/T snv 1.0E-02 3