Original source

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

Alleles
C/A|Ancestral: C|Ambiguity code: M|MAF: 0.24 (A)
Location

Chromosome 14:104793397 (forward strand)|View in location tab

Co-located variant

HGMD-PUBLIC CR108282

Most severe consequence
 
5 prime UTR variant
Evidence status

Synonyms
HGVS names

This variant has 12 HGVS names - Show

Genotyping chips

This variant has assays on 6 chips - Show

About this variant

This variant overlaps 11 transcripts, 1 regulatory feature, has 4134 sample genotypes and is mentioned in 43 citations.

Variant displays