Original source

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

HGMD-PUBLIC CS066643

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs58448806

HGVS names

This variant has 5 HGVS names - Show

About this variant

This variant overlaps 4 transcripts, has 2780 sample genotypes and is mentioned in 1 citation.

Variant displays