Original source

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

Alleles
G/C | Ancestral: G | Ambiguity code: S | MAF: 0.02 (C)
Location

Chromosome 20:58651187 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

20:g.58651187G>C

About this variant

This variant overlaps 22 transcripts and has 2505 individual genotypes.

Variation displays