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rs141733599

From SNPedia
ClinVar
Risk rs141733599(T;T)
Alt rs141733599(T;T)
Reference rs141733599(C;C)
Significance Other
Disease ALBUMIN LARINO
Variation info
Gene ALB
CLNDBN ALBUMIN LARINO
Reversed 0
HGVS NC_000004.11:g.74270123C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000019887.2,


[PMID 8022807OA-icon.png] Genetic variants of human serum albumin in Italy: point mutants and a carboxyl-terminal variant.