Original source

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

Alleles
-/G
Location

Chromosome 18: between 51058149 and 51058150 (forward strand) | View in location tab

Co-located

with COSMIC COSM1158484 (-/C), COSM85615 (-/G)

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB SCV000042357, SCV000042358

This variation has 13 HGVS names - click the plus to show

Variation displays