Original source

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

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

Chromosome 16:67809271 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

This variant has 16 HGVS names - click the plus to show

About this variant

This variant overlaps 24 transcripts and has 3 sample genotypes.

Variant displays