Original source

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

Alleles
-/A/AC/ACAC/C
Location

Chromosome 16: between 46681032 and 46681033 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms
HGVS names

This variant has 24 HGVS names - Show

About this variant

This variant overlaps 40 transcripts and has 4 sample genotypes.

Variant displays