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 20:45354069 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM080543

Most severe consequence
Clinical significance

Synonyms

LSDB 13568

This variation has 3 HGVS names - click the plus to show

20:g.45354069C>T
ENST00000359271.2:c.394C>T
ENSP00000352216.2:p.Arg132Trp

Variation displays