Original source

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

Alleles
T/C|Ancestral: T|Ambiguity code: Y|MAF: 0.09 (C)
Location

Chromosome 3:118482382 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs17676327, rs58538112

HGVS names

This variant has 2 HGVS names - Hide

3:g.118482382T>C
ENST00000482142.5:n.232+14241A>G

Genotyping chips

This variant has assays on 10 chips - Show

About this variant

This variant overlaps 1 transcript, has 3762 sample genotypes and is mentioned in 1 citation.

Variant displays