Product Details

SNP ID

rs35836460

Assay Type

Functionally tested

NCBI dbSNP Submissions

19

Location

Chr.1:196651923 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GAGTGCAGTGAGAATTGGGTTTAAC[C/T]TCTGGCATTTCTGGGCTTGTGGCTT

Phenotype

MIM: 134370

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

CFH PubMed Links

Gene Details

Gene

CFH

Gene Name

complement factor H

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_000186.3	46	UTR 5			NP_000177.2
NM_001014975.2	46	UTR 5			NP_001014975.1
XM_017001108.1	46	Intron			XP_016856597.1

View Full Product Details