Original source

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

Alleles
T/G|Ancestral: T|Ambiguity code: K
Location

Chromosome 2:27309707 (forward strand)|View in location tab

Most severe consequence
 
3 prime UTR variant
Evidence status

Synonyms

Archive dbSNP rs3189966

HGVS names

This variant has 10 HGVS names - Show

About this variant

This variant overlaps 25 transcripts and has 1 sample genotype.

Variant displays