Original source

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

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

Chromosome 5:148120063 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM001400 ; PhenCode SPINK5base_D0080:g.57019C>T (C/T)

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 12921

This variation has 12 HGVS names - click the plus to show

Variation displays