Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

Alleles
C/A|Ancestral: C|Ambiguity code: M|MAF: 0.13 (A)
Location

Chromosome 4:47320202 (forward strand)|View in location tab

Most severe consequence
 
Synonymous variant
Evidence status

Synonyms
HGVS names

This variant has 4 HGVS names - Show

Genotyping chips

This variant has assays on 10 chips - Show

About this variant

This variant overlaps 2 transcripts, has 5688 sample genotypes, is associated with 1 phenotype and is mentioned in 2 citations.

Variant displays