Original source

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

Alleles
ATTC/-
Location

Chromosome 1:12170193-12170196 (forward strand)|View in location tab

Co-located variant

dbSNP rs397844175 (ATTC/-)

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs56828712

HGVS names

This variant has 4 HGVS names - Show

About this variant

This variant overlaps 4 transcripts and 1 regulatory feature.

Variant displays