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 19:10133368 (forward strand) | View in location tab

Most severe consequence
 
3 prime UTR variant
Evidence status

Synonyms

Archive dbSNP rs3209915

This variant has 9 HGVS names - click the plus to show

About this variant

This variant overlaps 10 transcripts and has 1 sample genotype.

Variant displays