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: 0.43 (G)
Location

Chromosome 9:22124478 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

9:g.22124478A>G

This variation has assays on 5 chips - click the plus to show

About this variant

This variant overlaps 11 transcripts, has 1335 individual genotypes, is associated with 1 phenotype and is mentioned in 141 citations.

Variation displays