Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|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

HGVS names

This variant has 9 HGVS names - Show

About this variant

This variant overlaps 10 transcripts and has 1 sample genotype.

Variant displays