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

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB SCV000042357, SCV000042358

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

Variation displays