Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 19
rs763092306
CERKL ; NEUROD1
1.000 0.080 2 181678533 missense variant C/T snv 2
rs766982432
HNF1A
12 120994315 frameshift variant C/-;CC;CCC delins 1
rs780518365
HNF1A
12 120992362 intron variant A/G snv 1
rs201938902
ITGAD
16 31424046 non coding transcript exon variant A/G snv 0.26 1
rs752992795
N4BP1
16 48548859 intron variant T/A snv 4.1E-04 1
rs141627694
SLC5A2
16 31488637 missense variant T/C snv 6.6E-05 1.0E-04 1