Original source

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

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

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

Most severe consequence
Evidence status

Synonyms

HbVar 3

This variation has 5 HGVS names - click the plus to show

About this variant

This variant overlaps 10 transcripts and is mentioned in 2 citations.

Variation displays