rs376209366
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
T
Chromosome
19
Location
7556650
Variant Type
SNP
Genes
ClinVar
Name
NM_001166114.2(PNPLA6):c.3211-5C>T
Allele
T
Clinical Significance
Likely benign
C
T
19
7556650
SNP
NM_001166114.2(PNPLA6):c.3211-5C>T
T
Likely benign