Original source

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

Alleles
A/G | Ancestral: G | Ambiguity code: R | MAF: 0.11 (A)
Location

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

Most severe consequence
 
Synonymous variant
Evidence status

Synonyms

Archive dbSNP rs59467477

This variant has 7 HGVS names - click the plus to show

This variant has assays on 4 chips - click the plus to show

About this variant

This variant overlaps 6 transcripts, has 3744 sample genotypes and is mentioned in 4 citations.

Variant displays