Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R
Location

Chromosome 16:3150279 (forward strand) | View in location tab

Most severe consequence
 
Downstream gene variant
Evidence status

HGVS name

16:g.3150279G>A

About this variant

This variant overlaps 3 transcripts and 1 regulatory feature.

Variant displays