Original source

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

Alleles
T/C|Ancestral: T|Ambiguity code: Y|MAF: 0.10 (C)
Location

Chromosome 3:142449776 (forward strand)|View in location tab

Most severe consequence
 
3 prime UTR variant
Evidence status

Synonyms

Archive dbSNP rs59949967

HGVS names

This variant has 5 HGVS names - Show

About this variant

This variant overlaps 12 transcripts and has 2509 sample genotypes.

Variant displays