Original source

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

Alleles
G/A|Ancestral: G|Ambiguity code: R|MAF: 0.06 (A)
Location

Chromosome 4:110617671 (forward strand)|View in location tab

Co-located variant

HGMD-PUBLIC CR043663

Most severe consequence
 
3 prime UTR variant
Evidence status

Clinical significance

Synonyms

This variant has 2 synonyms - Show

HGVS names

This variant has 10 HGVS names - Show

Genotyping chips

This variant has assays on 7 chips - Show

About this variant

This variant overlaps 15 transcripts, has 3545 sample genotypes and is associated with 1 phenotype.

Variant displays