Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
A/G | Ancestral: A | Ambiguity code: R | MAF: 0.21 (G)
Location

Chromosome 4:47406692 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

This variation has 2 HGVS names - click the plus to show

This variation has assays on 9 chips - click the plus to show

About this variant

This variant overlaps 2 transcripts, has 3633 individual genotypes, is associated with 1 phenotype and is mentioned in 5 citations.

Variation displays