Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y
Location

Chromosome 9:99149252 (forward strand) | View in location tab

Co-located

with COSMIC COSM199708 (C/T) ; HGMD-PUBLIC CM064321

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 5766

This variation has 10 HGVS names - click the plus to show

Variation displays