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 16:57541217 (forward strand)|View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

HGVS name

16:g.57541217C>A

About this variant

This variant overlaps 7 transcripts, 1 regulatory feature and has 2 sample genotypes.

Variant displays