Original source

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

Alleles
G/C | Ancestral: C | Ambiguity code: S | MAF: 0.43 (C)
Location

Chromosome 9:22125504 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms
HGVS name

9:g.22125504G>C

This variation has assays on 7 chips - click the plus to show

About this variant

This variant overlaps 10 transcripts, has 2635 individual genotypes, is associated with 8 phenotypes and is mentioned in 159 citations.

Variation displays