Original source

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

Alleles
G/C | Ancestral: C | Ambiguity code: S | MAF: 0.22 (C)
Location

Chromosome 20:5315842 (forward strand) | View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

Synonyms

Archive dbSNP rs386620531, rs17721327

HGVS name

20:g.5315842G>C

This variant has assays on 4 chips - click the plus to show

About this variant

This variant overlaps 1 transcript and has 3112 sample genotypes.

Variant displays