rs5491
- risk factor
Your Genotype
Sign InDescription
Reference Allele
A
Alternative Allele
G
T
Chromosome
19
Location
10274864
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_000201.3(ICAM1):c.167A>T (p.Lys56Met)
Allele
T
Clinical Significance
risk factor