Original source

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

A/C | Ancestral: C | Ambiguity code: M | MAF: 0.17 (A)

Chromosome 19:5839602 (forward strand) | View in location tab

Most severe consequence
5 prime UTR variant
Evidence status


Archive dbSNP rs17748601, rs57750337

HGVS names

This variant has 5 HGVS names - Show

Genotyping chips

This variant has assays on 5 chips - Show

About this variant

This variant overlaps 17 transcripts and has 3888 sample genotypes.

Variant displays