Original source

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

Alleles
A/G|Ancestral: G|Ambiguity code: R|MAF: 0.42 (A)
Location

Chromosome 20:46727347 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs3091927, rs57711433

HGVS names

This variant has 2 HGVS names - Show

About this variant

This variant overlaps 2 transcripts, has 2508 sample genotypes and is mentioned in 1 citation.

Variant displays