Original source

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

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

Chromosome 16:23181594 (forward strand) | View in location tab

Most severe consequence
 
Upstream gene variant
HGVS name

16:g.23181594A>G

About this variant

This variant overlaps 1 transcript.

Variant displays