Original source

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

Alleles
C/A|Ancestral: C|Ambiguity code: M
Location

Chromosome 16:172929 (forward strand)|View in location tab

Most severe consequence
 
Missense variant
Evidence status

Synonyms

LSDB HbVar.3

HGVS names

This variant has 5 HGVS names - Show

About this variant

This variant overlaps 9 transcripts, 1 regulatory feature and is mentioned in 2 citations.

Variant displays