Original source

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

Alleles
G/C|Ancestral: G|Ambiguity code: S|MAF: 0.42 (C)
Location

Chromosome 20:54153053 (forward strand)|View in location tab

Most severe consequence
 
Downstream gene variant
Evidence status

Synonyms

Archive dbSNP rs58925284

HGVS name

20:g.54153053G>C

About this variant

This variant overlaps 4 transcripts, 1 regulatory feature, has 2779 sample genotypes and is mentioned in 1 citation.

Variant displays