Original source

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

Alleles
A/C | Ancestral: A | Ambiguity code: M | MAF: 0.02 (C)
Location

Chromosome 20:9067837 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs58375760

HGVS name

20:g.9067837A>C

About this variant

This variant overlaps 6 transcripts and has 2776 individual genotypes.

Variation displays