Original source

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

A/T | Ancestral: A | Ambiguity code: W | MAF: 0.10 (T)

Chromosome 5:154475154 (forward strand) | View in location tab

Most severe consequence
3 prime UTR variant
Evidence status

HGVS names

This variant has 2 HGVS names - Show

About this variant

This variant overlaps 1 transcript and has 2510 sample genotypes.

Variant displays