Product Details

SNP ID

rs3748556

Assay Type

Functionally tested

NCBI dbSNP Submissions

36

Location

Chr.1:196957826 on Build GRCh38

Set Membership

HapMap JSNP

Context Sequence [VIC/FAM]

GATAGACTATAAAGTGCCTTGTTTG[C/T]ATTTGCCTTATTTGAACTTGTATTT

Phenotype

MIM: 600889

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

CFHR2 PubMed Links

Gene Details

Gene

CFHR2

Gene Name

complement factor H related 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001312672.1		Intron			NP_001299601.1
NM_005666.3		Intron			NP_005657.1
XM_005245113.3		Intron			XP_005245170.1
XM_011509458.2		Intron			XP_011507760.1
XM_011509459.2		Intron			XP_011507761.1
XM_011509460.2		Intron			XP_011507762.1
XM_017001109.1		Intron			XP_016856598.1

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