Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | 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

This variant has 35 HGVS names - click the plus to show

About this variant

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

Variant displays