Original source

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

Alleles
-/A|MAF: 0.17 (-)
Location

Chromosome 16: between 46675010 and 46675011 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms
HGVS names

This variant has 4 HGVS names - Show

About this variant

This variant overlaps 6 transcripts and has 2514 sample genotypes.

Variant displays