Original source

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

Alleles
T/C|Ancestral: C|Ambiguity code: Y|MAF: 0.22 (T)
Location

Chromosome 4:6302515 (forward strand)|View in location tab

Most severe consequence
 
3 prime UTR variant
Evidence status

Synonyms

Archive dbSNP rs56689134, rs3172623

HGVS names

This variant has 4 HGVS names - Show

Genotyping chips

This variant has assays on 6 chips - Show

About this variant

This variant overlaps 5 transcripts, has 3763 sample genotypes and is mentioned in 1 citation.

Variant displays