rs75423111
- Benign
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
C
Chromosome
9
Location
112149311
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_022486.5(SUSD1):c.306C>T (p.Cys102=)
Allele
A
Clinical Significance
Benign