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: < 0.01 (A)
Location

Chromosome 22:36293787 (forward strand) | View in location tab

Co-located

with COSMIC COSM1416045 (G/A)

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB NC_000022.9:g.35019779G>A

This variation has 3 HGVS names - click the plus to show

Variation displays