Original source

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

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

Chromosome 14:20940525 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM981389 ; PhenCode NPbase_D0064:g.3957C>T (C/T)

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 4324, 2010_April_001_039_NP_164050_0008

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

Variation displays