Original source

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

A/G | Ancestral: A | Ambiguity code: R

Chromosome 17:7669095 (forward strand) | View in location tab

Most severe consequence
3 prime UTR variant
Evidence status


Archive dbSNP rs1042534

HGVS names

This variant has 35 HGVS names - Show

About this variant

This variant overlaps 36 transcripts, has 2 sample genotypes and is mentioned in 1 citation.

Variant displays