Original source

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

Alleles
T/C|Ancestral: T|Ambiguity code: Y
Location

Chromosome 16:176701 (forward strand)|View in location tab

Co-located variant

PhenCode HbVar.1178 (T/C)

Most severe consequence
 
5 prime UTR variant
Evidence status

Synonyms

LSDB HbVar.1178

HGVS names

This variant has 3 HGVS names - Show

About this variant

This variant overlaps 10 transcripts and 2 regulatory features.

Variant displays