Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | 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
Evidence status

Synonyms
HGVS name

4:g.154613256T>C

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

About this variant

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

Variation displays