Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9349205
CCND3
6 41957421 intron variant G/A;C snv 6
rs3218097
CCND3
6 41937537 intron variant G/A;T snv 5
rs112233623
CCND3
6 41957260 intron variant C/T snv 7.0E-03 5
rs9394841
CCND3
6 41959197 intron variant T/C snv 0.22 3
rs67289879
CCND3
1.000 0.040 6 42039665 intron variant C/A;G;T snv 2
rs33966734
CCND3
6 41936060 stop gained C/A;G;T snv 1.2E-02; 4.0E-06 2
rs10947997
CCND3
6 41953503 intron variant G/T snv 0.13 2
rs3218092
CCND3
6 41938923 intron variant A/G snv 0.18 2
rs4554318
CCND3
6 42044421 intron variant C/T snv 0.55 2
rs143111788
CCND3
6 41951438 intron variant AGCTACTC/- delins 0.59 2
rs11970772
CCND3
6 41957552 intron variant T/A snv 0.24 2
rs9296369
CCND3
6 41953258 intron variant C/G;T snv 2
rs16895130
CCND3
6 41957193 intron variant A/G snv 0.22 2
rs144387335
CCND3 ; LOC105375059
6 42010872 non coding transcript exon variant CTT/- delins 0.18 2
rs56144648
LOC105375059 ; CCND3
6 42021004 intron variant G/A snv 0.18 2
rs1410492
CCND3
6 41940117 intron variant G/A;C snv 1
rs113267280
CCND3
6 41984773 intron variant T/G snv 7.3E-03 1
rs4714556
CCND3
6 42025491 intron variant A/G snv 0.39 1
rs4130023
CCND3
6 41966776 intron variant C/T snv 0.17 1
rs9349204
CCND3
6 41946640 intron variant A/G;T snv 1
rs9369327
CCND3
6 42046566 intron variant C/T snv 6.5E-02 1
rs4714548
CCND3 ; LOC105375059
6 42015693 intron variant A/C;G;T snv 1
rs9367125
CCND3 ; LOC105375059
6 42019806 intron variant G/C snv 0.10 1
rs182679717
CCND3 ; LOC105375060
6 42007955 intron variant C/A;T snv 1
rs9381118
LOC105375059 ; CCND3
6 42017698 intron variant T/C snv 0.72 1