Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
C/T | Ancestral: T | Ambiguity code: Y | MAF: 0.46 (C)
Location

Chromosome 20:44111397 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs58231880

This variation has 2 HGVS names - click the plus to show

About this variant

This variant overlaps 2 transcripts and has 2513 individual genotypes.

Variation displays