Original source

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

Synonyms

Archive dbSNP rs58828399, rs3805662

This variation has 5 HGVS names - click the plus to show

About this variant

This variant overlaps 10 transcripts, has 2564 individual genotypes and is mentioned in 1 citation.

Variation displays