Original source

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

Alleles
-/G
Location

Chromosome 18: between 48584519 and 48584520 (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