Original source

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

Alleles
G/A/C | Ancestral: G | Ambiguity code: V
Location

Chromosome 9:99149253 (forward strand) | View in location tab

Co-located

with COSMIC COSM1635939 (G/A) ; HGMD-PUBLIC CM063198, CM050757

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 5763, 5765

This variation has 20 HGVS names - click the plus to show

Variation displays