rs73419888
- Benign
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
C
T
Chromosome
22
Location
38069027
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_012407.4(PICK1):c.350-6G>A
Allele
A
Clinical Significance
Benign
G
A
C
T
22
38069027
SNP
NM_012407.4(PICK1):c.350-6G>A
A
Benign