Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|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 4 transcripts and 1 regulatory feature.

Variant displays