Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.44 (T)
Location

Chromosome 3:87273910 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CS066643

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs58448806

This variant has 5 HGVS names - click the plus to show

About this variant

This variant overlaps 4 transcripts, has 2543 sample genotypes and is mentioned in 1 citation.

Variant displays