rs773527127
- Uncertain significance
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
A
T
Chromosome
11
Location
65720644
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_032193.4(RNASEH2C):c.115G>T (p.Asp39Tyr)
Allele
A
Clinical Significance
Uncertain significance
Name
NM_032193.4(RNASEH2C):c.115G>A (p.Asp39Asn)
Allele
T
Clinical Significance
Uncertain significance