Original source

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

Alleles
A/G|Ancestral: G|Ambiguity code: R|MAF: 0.30 (A)
Location

Chromosome 4:76001835 (forward strand)|View in location tab

Most severe consequence
 
3 prime UTR variant
Evidence status

Synonyms
HGVS names

This variant has 3 HGVS names - Show

Genotyping chips

This variant has assays on 5 chips - Show

About this variant

This variant overlaps 2 transcripts, 1 regulatory feature, has 4030 sample genotypes and is mentioned in 7 citations.

Variant displays