Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP

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

Chromosome 10:89720852 (forward strand) | View in location tab

Co-located

with COSMIC COSM5151 (C/T), COSM921156 (C/G) ; HGMD-PUBLIC CM971278

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB Cosmic:5151, 10487

This variation has 7 HGVS names - click the plus to show

Variation displays