Original source

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

Alleles
G/T | Ancestral: G | Ambiguity code: K
Location

Chromosome 3:170996771 (forward strand) | View in location tab

Most severe consequence
 
3 prime UTR variant
Evidence status

Synonyms

Archive dbSNP rs62623382

This variant has 2 HGVS names - click the plus to show

About this variant

This variant overlaps 4 transcripts and 1 regulatory feature.

Variant displays