Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

Alleles
G/C | Ancestral: G | Ambiguity code: S | MAF: 0.40 (C)
Location

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

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs58925284

HGVS name

20:g.54153053G>C

About this variant

This variant overlaps 5 transcripts, has 1380 individual genotypes and is mentioned in 1 citation.

Variation displays