Original source

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

Alleles
C/T | Ancestral: T | Ambiguity code: Y | MAF: 0.14 (T)
Location

Chromosome 4:154569680 (forward strand) | View in location tab

Most severe consequence
 
Synonymous variant
Evidence status

Synonyms

This variant has 4 HGVS names - click the plus to show

This variant has assays on 7 chips - click the plus to show

About this variant

This variant overlaps 7 transcripts, has 4003 sample genotypes and is mentioned in 2 citations.

Variant displays