Original source

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

Alleles
A/T | Ancestral: A | Ambiguity code: W
Location

Chromosome 2:220286216 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM980539 ; PhenCode DES:c.1178A>T (A/T)

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB DES:c.[1078G>C; 1178A>T], 1536

This variation has 8 HGVS names - click the plus to show

Variation displays