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
ENST00000584020.4:n.261-12031G>A
ENST00000584351.4:n.846+1734G>A
ENST00000584816.4:n.261-12031G>A
ENST00000455933.5:n.68-12031G>A
ENST00000585267.4:n.372-12031G>A
ENST00000582301.4:n.261-12031G>A
ENST00000581051.4:n.261-12031G>A
ENST00000580467.4:n.372-12031G>A
ENST00000577551.4:n.261-12031G>A
ENST00000584637.4:n.261-12031G>A
ENST00000582072.4:n.261-12031G>A
ENST00000428597.4:n.846+1734G>A
ENST00000580576.4:n.533+5126G>A
ENST00000583719.4:n.372-12031G>A

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

About this variant

This variant overlaps 16 transcripts, has 2285 individual genotypes, is associated with 1 phenotype and is mentioned in 8 citations.

Variation displays