Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11071720
TPM1-AS ; TPM1
15 63049797 intron variant T/C;G snv 3
rs11082304
CABLES1
18 23141009 intron variant G/C;T snv 5
rs11121012
CAMTA1
1 7734229 intron variant A/G snv 0.62 2
rs11121529
KIF1B
1 10211630 5 prime UTR variant C/G snv 0.20 1
rs11123694
GCC2
2 108448107 upstream gene variant C/T snv 0.39 1
rs111896493
ADGRE5
19 14381256 5 prime UTR variant -/AGTG delins 1
rs112346425
AP2B1
17 35680792 intron variant G/C;T snv 1
rs11235688
P2RY2
11 73236889 upstream gene variant G/A;C snv 1
rs112505971
ANKRD26
10 27068541 intron variant A/C;G snv 13
rs11315757
PPP4R1-AS1
18 9617722 intron variant AA/-;A;AAA;AAAA delins 1
rs11356207 17 64307290 downstream gene variant TTTT/-;T;TT;TTT;TTTTT delins 0.49 1
rs11459029
ARHGEF3
3 56740187 intron variant -/A delins 1
rs114694170
MEF2C ; MEF2C-AS1
1.000 0.040 5 88884379 non coding transcript exon variant T/C snv 3.6E-02 4
rs11471957
TUBB1
20 59023277 intron variant -/AA ins 2
rs11477536
DNTTIP1
20 45796388 intron variant AAAA/-;A;AA;AAA;AAAAA;AAAAAA delins 1
rs11540084
LOC107985305 ; PVR
19 44644040 5 prime UTR variant G/T snv 0.26 1
rs11553699
TMEM120B ; RHOF
12 121779004 3 prime UTR variant A/G snv 9.4E-02 6
rs11593377
PROSER2-AS1 ; PROSER2
10 11853098 intron variant T/C;G snv 1
rs11601507
TRIM5
1.000 0.040 11 5679844 missense variant C/A;T snv 9.3E-02; 4.0E-06 3
rs11602954
BET1L
11 202856 intron variant G/A snv 0.17 2
rs11604127
ODF3 ; BET1L
11 196944 5 prime UTR variant C/T snv 0.17 2
rs11627485
FNTB ; CHURC1-FNTB ; MAX
14 65020976 intron variant T/C snv 0.36 5
rs11627756
RCOR1
14 102630269 intron variant C/T snv 0.62 1
rs116383353
TBC1D14
4 6923070 intron variant G/A;T snv 1
rs11653144 17 29348208 upstream gene variant C/T snv 0.43 1