Original source

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

Alleles
T/C|Ancestral: T|Ambiguity code: Y|MAF: 0.16 (C)
Location

Chromosome 14:64233327 (forward strand)|View in location tab

Co-located variant

HGMD-PUBLIC CS067819

Most severe consequence
 
Splice region variant
Evidence status

Synonyms

Archive dbSNP rs58894804

HGVS names

This variant has 13 HGVS names - Show

Genotyping chips

This variant has assays on 8 chips - Show

About this variant

This variant overlaps 13 transcripts, 1 regulatory feature, has 3692 sample genotypes and is mentioned in 4 citations.

Variant displays