Original source

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

A/C | Ancestral: A | Ambiguity code: M | MAF: 0.38 (A)

Chromosome 19:41350981 (forward strand) | View in location tab

Most severe consequence
5 prime UTR variant
Evidence status


This variant has 3 synonyms - Show

HGVS names

This variant has 4 HGVS names - Show

Genotyping chips

This variant has assays on 9 chips - Show

About this variant

This variant overlaps 7 transcripts, 1 regulatory feature, has 3962 sample genotypes and is mentioned in 9 citations.

Variant displays