Source: CURATED

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1983023
rs1983023
2 233728376 intron variant T/C snv 0.46
CUI: C1287365
Disease: Bilirubin level result
Bilirubin level result
0.700 1.000 1 2009 2009
dbSNP: rs1983023
rs1983023
2 233728376 intron variant T/C snv 0.46
CUI: C0344395
Disease: Bilirubin measurement
Bilirubin measurement
0.700 1.000 1 2009 2009
dbSNP: rs1983023
rs1983023
2 233728376 intron variant T/C snv 0.46
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2013 2013
dbSNP: rs2008595
rs2008595
2 233728546 intron variant C/T snv 0.56
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2013 2013
dbSNP: rs2008595
rs2008595
2 233728546 intron variant C/T snv 0.56
CUI: C1287365
Disease: Bilirubin level result
Bilirubin level result
0.700 1.000 1 2009 2009
dbSNP: rs2008595
rs2008595
2 233728546 intron variant C/T snv 0.56
CUI: C0344395
Disease: Bilirubin measurement
Bilirubin measurement
0.700 1.000 1 2009 2009
dbSNP: rs3806597
rs3806597
2 233728923 intron variant A/G snv 0.56
CUI: C1287365
Disease: Bilirubin level result
Bilirubin level result
0.700 1.000 2 2009 2013
dbSNP: rs3806597
rs3806597
2 233728923 intron variant A/G snv 0.56
CUI: C0344395
Disease: Bilirubin measurement
Bilirubin measurement
0.700 1.000 2 2009 2013
dbSNP: rs3806597
rs3806597
2 233728923 intron variant A/G snv 0.56
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2013 2013
dbSNP: rs3806596
rs3806596
2 233729061 intron variant T/C snv 0.56
CUI: C0344395
Disease: Bilirubin measurement
Bilirubin measurement
0.700 1.000 2 2009 2013
dbSNP: rs3806596
rs3806596
2 233729061 intron variant T/C snv 0.56
CUI: C1287365
Disease: Bilirubin level result
Bilirubin level result
0.700 1.000 2 2009 2013
dbSNP: rs3806596
rs3806596
2 233729061 intron variant T/C snv 0.56
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2013 2013
dbSNP: rs28898617
rs28898617
1.000 0.040 2 233729143 missense variant A/G snv 3.5E-03 1.1E-03
CUI: C0344395
Disease: Bilirubin measurement
Bilirubin measurement
0.700 1.000 1 2018 2018
dbSNP: rs17868336
rs17868336
2 233729360 synonymous variant A/G snv 2.3E-02 2.6E-02
CUI: C0344395
Disease: Bilirubin measurement
Bilirubin measurement
0.700 1.000 1 2009 2009
dbSNP: rs17868336
rs17868336
2 233729360 synonymous variant A/G snv 2.3E-02 2.6E-02
CUI: C1287365
Disease: Bilirubin level result
Bilirubin level result
0.700 1.000 1 2009 2009
dbSNP: rs7574296
rs7574296
2 233729603 synonymous variant A/G snv 0.49 0.54
CUI: C0344395
Disease: Bilirubin measurement
Bilirubin measurement
0.700 1.000 1 2009 2009
dbSNP: rs7574296
rs7574296
2 233729603 synonymous variant A/G snv 0.49 0.54
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2013 2013
dbSNP: rs7574296
rs7574296
2 233729603 synonymous variant A/G snv 0.49 0.54
CUI: C1287365
Disease: Bilirubin level result
Bilirubin level result
0.700 1.000 1 2009 2009
dbSNP: rs11891311
rs11891311
2 233730664 intron variant G/A snv 0.42
CUI: C1287365
Disease: Bilirubin level result
Bilirubin level result
0.700 1.000 4 2009 2013
dbSNP: rs11891311
rs11891311
2 233730664 intron variant G/A snv 0.42
CUI: C0344395
Disease: Bilirubin measurement
Bilirubin measurement
0.800 1.000 4 2009 2013
dbSNP: rs11891311
rs11891311
2 233730664 intron variant G/A snv 0.42
CUI: C0489786
Disease: Height
Height
0.700 1.000 1 2010 2010
dbSNP: rs11891311
rs11891311
2 233730664 intron variant G/A snv 0.42
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2013 2013
dbSNP: rs17868337
rs17868337
2 233731010 intron variant G/A snv 1.6E-02
CUI: C0344395
Disease: Bilirubin measurement
Bilirubin measurement
0.700 1.000 1 2009 2009
dbSNP: rs17868337
rs17868337
2 233731010 intron variant G/A snv 1.6E-02
CUI: C1287365
Disease: Bilirubin level result
Bilirubin level result
0.700 1.000 1 2009 2009
dbSNP: rs75520741
rs75520741
2 233732958 intron variant C/G;T snv
CUI: C0344395
Disease: Bilirubin measurement
Bilirubin measurement
0.700 1.000 1 2018 2018