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: 0.27 (A)
Location

Chromosome 9:72700522 (forward strand) | View in location tab

Most severe consequence
Evidence status

Clinical significance

This variation has 5 synonyms - click the plus to show

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

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

About this variant

This variant overlaps 2 transcripts, has 2343 individual genotypes, is associated with 1 phenotype and is mentioned in 1 citation.

Variation displays