Original source

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

Alleles
A/G | Ancestral: A | Ambiguity code: R | MAF: 0.23 (G)
Location

Chromosome 22:40256869 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs58057376

This variant has 5 HGVS names - click the plus to show

22:g.40256869A>G
ENST00000454349.6:c.116-4963A>G
ENST00000402203.5:c.224-4963A>G
ENST00000301923.13:c.224-4963A>G
ENST00000335727.13:c.116-4963A>G

This variant has assays on 11 chips - click the plus to show

About this variant

This variant overlaps 4 transcripts, has 3957 sample genotypes, is associated with 1 phenotype and is mentioned in 5 citations.

Variant displays