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 9:122204712 (forward strand) | View in location tab

Most severe consequence
 
Missense variant
Evidence status

Synonyms

Archive dbSNP rs3206376

This variant has 13 HGVS names - click the plus to show

About this variant

This variant overlaps 11 transcripts, 1 regulatory feature and has 1 sample genotype.

Variant displays