Original source

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

Alleles
A/G|Ancestral: A|Ambiguity code: R|MAF: 0.31 (G)
Location

Chromosome 18:44869650 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs58137141

HGVS names

This variant has 3 HGVS names - Show

About this variant

This variant overlaps 2 transcripts and has 2513 sample genotypes.

Variant displays