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 16:88812533 (forward strand)|View in location tab

Most severe consequence
 
Upstream gene variant
HGVS name

16:g.88812533C>A

About this variant

This variant overlaps 16 transcripts and 1 regulatory feature.

Variant displays