Original source

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

This variant has 4 HGVS names - click the plus to show

About this variant

This variant overlaps 6 transcripts and has 2514 sample genotypes.

Variant displays