Original source

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

Alleles
G/A/C | Ancestral: G | Ambiguity code: V
Location

Chromosome 17:17118542 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM023465

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 14742

This variation has 14 HGVS names - click the plus to show

Variation displays