Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP

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

Chromosome 22:40652873 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs58057376

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

22:g.40652873A>G
ENST00000454349.2:c.116-4963A>G
ENST00000402203.1:c.224-4963A>G
ENST00000301923.9:c.224-4963A>G
ENST00000335727.9:c.116-4963A>G

This variation has assays on 9 chips - click the plus to show

Variation displays