Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs11045626
rs11045626
12 20965963 intron variant A/G snv 0.14
CUI: C1287365
Disease: Bilirubin level result
Bilirubin level result
0.700 1.000 1 2009 2009
dbSNP: rs11045627
rs11045627
12 20966129 intron variant C/G;T snv
CUI: C1287365
Disease: Bilirubin level result
Bilirubin level result
0.700 1.000 1 2009 2009
dbSNP: rs11045630
rs11045630
12 20972587 intron variant T/C snv 0.14
CUI: C1287365
Disease: Bilirubin level result
Bilirubin level result
0.700 1.000 1 2009 2009
dbSNP: rs12825142
rs12825142
12 20972738 intron variant C/G snv 0.14
CUI: C1287365
Disease: Bilirubin level result
Bilirubin level result
0.700 1.000 1 2009 2009
dbSNP: rs1910196
rs1910196
12 20964279 intron variant G/A snv 0.47
CUI: C1287365
Disease: Bilirubin level result
Bilirubin level result
0.700 1.000 1 2009 2009
dbSNP: rs2417873
rs2417873
12 21013389 intron variant G/A snv 0.40
CUI: C1287365
Disease: Bilirubin level result
Bilirubin level result
0.700 1.000 1 2009 2009