Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs113760175
CASC15
6 22343363 intron variant G/A;T snv 3
rs113977268
CASC15 ; LOC105374971
6 22359286 intron variant G/A snv 5.7E-02 2
rs141007801
CASC15
6 21722558 intron variant A/-;AA;AAA;AAAA delins 2
rs2744132
LOC105374971 ; CASC15
6 22392594 intron variant G/A snv 0.14 1
rs6926491
CASC15
6 21724439 intron variant G/A snv 0.21 1
rs10484389
CASC15
6 22075033 intron variant C/T snv 6.0E-02 1
rs67258057
CASC15
6 21948833 intron variant G/A snv 4.8E-02 1
rs6903716
CASC15
6 21956173 intron variant A/G snv 0.30 1
rs7763264
CASC15
6 21959834 intron variant C/G;T snv 1
rs1928175
CASC15
6 22079256 intron variant G/A snv 0.55 1
rs3736675
CASC15
6 22110919 splice region variant G/A snv 3.0E-02 1
rs1928168
CASC15
6 22017509 intron variant T/C snv 0.36 1
rs2078543
CASC15
6 21996631 intron variant A/G snv 0.69 1
rs112204664
CASC15
6 21867474 intron variant G/A snv 0.13 1
rs74360995
CASC15
6 21886258 non coding transcript exon variant T/C snv 0.12 1
rs1205896
CASC15
6 22341240 intron variant G/A snv 0.47 1
rs9393294
LOC105374971 ; CASC15
6 22465392 intron variant C/T snv 0.13 1
rs12525417
CASC15
6 22591478 intron variant C/T snv 0.33 1
rs2744133
LOC105374971 ; CASC15
6 22392031 intron variant A/G;T snv 1
rs6911827
CASC15
6 22130372 intron variant C/G;T snv 1
rs9466161
CASC15
6 21722685 intron variant T/C snv 0.25 1
rs7760082
CASC15
6 21919156 intron variant G/A snv 0.59 1
rs6934973
CASC15
6 21920795 intron variant A/G snv 0.32 1
rs13198081
CASC15
6 22017314 intron variant G/C snv 0.35 1
rs6939340
CASC15 ; NBAT1
0.851 0.160 6 22139775 intron variant A/G snv 0.62 1