rs1060501762
- Uncertain significance
- Uncertain significance
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
T
Alternative Allele
A
C
G
Chromosome
17
Location
61683963
Variant Type
SNP
Genes
ClinVar
Name
NM_032043.3(BRIP1):c.3083A>G (p.Asn1028Ser)
Allele
C
Clinical Significance
Uncertain significance
Name
NM_032043.3(BRIP1):c.3083A>C (p.Asn1028Thr)
Allele
G
Clinical Significance
Uncertain significance
Name
NM_032043.3(BRIP1):c.3083A>T (p.Asn1028Ile)
Allele
A
Clinical Significance
Uncertain significance