Original source

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

Alleles
A/T|Ancestral: T|Ambiguity code: W|MAF: 0.44 (A)
Location

Chromosome 5:135030100 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs58828399, rs3805662

HGVS names

This variant has 5 HGVS names - Show

About this variant

This variant overlaps 10 transcripts, has 3044 sample genotypes and is mentioned in 1 citation.

Variant displays