Original source

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

Alleles
C/G | Ancestral: G | Ambiguity code: S | MAF: 0.19 (C)
Location

Chromosome 22:50630089 (forward strand) | View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

Synonyms

Archive dbSNP rs58699285, rs5770954

HGVS name

22:g.50630089C>G

About this variant

This variant overlaps 7 transcripts and has 2690 sample genotypes.

Variant displays