Original source

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

This variant has 2 HGVS names - click the plus to show

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

This variant has assays on 6 chips - click the plus to show

About this variant

This variant overlaps 1 transcript, has 2649 sample genotypes, is associated with 2 phenotypes and is mentioned in 25 citations.

Variant displays