Original source

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

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

Chromosome 16:47666010 (forward strand) | View in location tab

Most severe consequence
 
Missense variant
Evidence status

Synonyms

This variant has 9 HGVS names - click the plus to show

About this variant

This variant overlaps 6 transcripts and has 2 sample genotypes.

Variant displays