Disorder "Neonatal Hyperbilirubinemia"
Found 1 record
Disorder information
Disorder name:
Neonatal Hyperbilirubinemia
Disoder ID:
Definition:
A type of hyperbilirubinemia with neonatal onset.
Modifier statisitcs
Record:
1
Gene:
1
Variant:
1
Reference:
1
Effect type:
Expressivity(1)
Modifier effect:
Risk factor(1)
| Modifier gene | Variant | Effect type | Modifier effect | Evidence | Effect | PubMed ID |
|---|---|---|---|---|---|---|
| UGT1A1 | UGT1A1:c.211G>A(p.Gly71Arg) | Expressivity | Risk factor | OR=2.17, P=0.02 for breastfeeding; OR=9.776, P=0.000 for ugta*6 Homozygote; OR=3.151, P=0.000 for ugta*6 heterozygote | A allele of rs4148323 (UGTA*6) were correlated with an increased risk of hyperbilirubinemiamore | more |
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