Original source

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

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

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

Most severe consequence
 
3 prime UTR variant
Evidence status

Synonyms

Archive dbSNP rs1042534

HGVS names

This variant has 36 HGVS names - Show

About this variant

This variant overlaps 37 transcripts, has 2 sample genotypes and is mentioned in 1 citation.

Variant displays