Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|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
 
Downstream gene variant
Evidence status

Synonyms

Archive dbSNP rs58231880

HGVS names

This variant has 2 HGVS names - Show

About this variant

This variant overlaps 2 transcripts and has 2513 sample genotypes.

Variant displays