rs75146158
- Pathogenic
Your Genotype
Sign InDescription
Reference Allele
T
Alternative Allele
A
C
Chromosome
11
Location
65720085
Variant Type
SNP
Phenotypes
ClinVar
Name
NM_032193.4(RNASEH2C):c.428A>T (p.Lys143Ile)
Allele
A
Clinical Significance
Pathogenic