Original source

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

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

Chromosome 17:48725633 (forward strand)|View in location tab

Most severe consequence
 
3 prime UTR variant
Evidence status

Synonyms

Archive dbSNP rs3169792

HGVS names

This variant has 4 HGVS names - Show

About this variant

This variant overlaps 8 transcripts and has 2 sample genotypes.

Variant displays