Product Details
- SNP ID
-
rs487114
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
28
- Location
-
Chr.1:196653771 on Build GRCh38
- Set Membership
-
HapMap
- Context Sequence [VIC/FAM]
- TTTATTTTTCATCAATGTGTGTTTA[A/C]ATGTGGTATCAGTTTCTACTGGTGA
- Phenotype
-
MIM: 134370
- Polymorphism
- A/C, Transversion substitution
- Allele Nomenclature
-
- Literature Links
-
CFH
PubMed Links
Gene Details
- Gene
- CFH
- Gene Name
- complement factor H
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