Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | 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

This variant has 2 HGVS names - click the plus to show

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

This variant has assays on 10 chips - click the plus to show

About this variant

This variant overlaps 1 transcript, has 2655 sample genotypes and is mentioned in 1 citation.

Variant displays