Original source

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

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

Chromosome 5:150879305 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs56583800, rs57988777

HGVS names

This variant has 2 HGVS names - Hide

5:g.150879305A>G
ENST00000520549.1:c.*79-280A>G

Genotyping chips

This variant has assays on 6 chips - Show

About this variant

This variant overlaps 1 transcript, has 3964 sample genotypes, is associated with 2 phenotypes and is mentioned in 25 citations.

Variant displays