Original source

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

Alleles
T/A | Ancestral: T | Ambiguity code: W
Location

Chromosome 6:143942226 (forward strand) | View in location tab

Most severe consequence
 
Missense variant
Evidence status

Synonyms

Archive dbSNP rs3173099

This variant has 20 HGVS names - click the plus to show

About this variant

This variant overlaps 19 transcripts, 1 regulatory feature and has 1 sample genotype.

Variant displays