Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [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
Evidence status

Synonyms

Archive dbSNP rs58057376

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

22:g.40256869A>G
ENST00000454349.4:c.116-4963A>G
ENST00000402203.3:c.224-4963A>G
ENST00000301923.11:c.224-4963A>G
ENST00000335727.11:c.116-4963A>G

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

Variation displays