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 16:50755151 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

This variant has 12 HGVS names - click the plus to show

About this variant

This variant overlaps 12 transcripts.

Variant displays