Original source

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

with HGMD-PUBLIC CR108282

Most severe consequence
 
5 prime UTR variant
Evidence status

Synonyms

This variant has 12 HGVS names - click the plus to show

This variant has assays on 6 chips - click the plus to show

About this variant

This variant overlaps 11 transcripts, 1 regulatory feature, has 4134 sample genotypes and is mentioned in 41 citations.

Variant displays