Original source

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

A/C/G | Ancestral: G | Ambiguity code: V | MAF: 0.11 (A)

Chromosome 4:148435364 (forward strand) | View in location tab

Most severe consequence
Missense variant
Evidence status


Archive dbSNP rs59467477

HGVS names

This variant has 26 HGVS names - Show

Genotyping chips

This variant has assays on 4 chips - Show

About this variant

This variant overlaps 12 transcripts, has 3744 sample genotypes and is mentioned in 4 citations.

Variant displays