Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs165599
rs165599
Entrez Id: 421;1312
Gene Symbol: ARVCF;COMT
ARVCF;COMT
CUI: C1611743
Disease:
Familial (FPAH)
0.010 GeneticVariation BEFREE DRD4 sites showed significant difference in allelic frequencies by case-control analysis, while DDC and COMT exhibited bias in familial transmission (P < 0.05). rs3837091 "AGAG," rs3735273 "A," rs1799732 "C," rs740603 "G," rs165599 "G" and single repeat alleles of rs4646984/rs4646983 showed positive correlation with co-morbid characteristics (P < 0.05). 24163823 2013