Original source

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

Alleles
T/C|Ancestral: T|Ambiguity code: Y|MAF: 0.30 (C)
Location

Chromosome 4:154613256 (forward strand)|View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

Synonyms
HGVS name

4:g.154613256T>C

Genotyping chips

This variant has assays on 9 chips - Show

About this variant

This variant overlaps 12 transcripts, has 4408 sample genotypes and is mentioned in 8 citations.

Variant displays