Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | View in dbSNP

Alleles
G/A | Ancestral: G | Ambiguity code: R | MAF: 0.47 (G)
Location

Chromosome 9:22034720 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs58620769

This variation has 15 HGVS names - click the plus to show

9:g.22034720G>A
ENST00000584020.2:n.261-12031G>A
ENST00000584816.2:n.261-12031G>A
ENST00000585267.2:n.372-12031G>A
ENST00000582301.2:n.261-12031G>A
ENST00000577551.2:n.261-12031G>A
ENST00000584637.2:n.261-12031G>A
ENST00000582072.2:n.261-12031G>A
ENST00000584351.2:n.846+1734G>A
ENST00000455933.3:n.68-12031G>A
ENST00000581051.2:n.261-12031G>A
ENST00000580467.2:n.372-12031G>A
ENST00000428597.2:n.846+1734G>A
ENST00000580576.2:n.533+5126G>A
ENST00000583719.2:n.372-12031G>A

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

Variation displays