Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

Alleles
G/C|Ancestral: G|Ambiguity code: S|MAF: 0.06 (C)
Location

Chromosome 18:5392026 (forward strand)|View in location tab

Most severe consequence
 
Downstream gene variant
Evidence status

Synonyms

Archive dbSNP rs57409652

HGVS name

18:g.5392026G>C

About this variant

This variant overlaps 10 transcripts and has 2507 sample genotypes.

Variant displays