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 3:122003260 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM021251 ; PhenCode CASRdb_c.2459C>G (C/G)

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_051_CASR_601199_0038, 10003

This variation has 7 HGVS names - click the plus to show

Variation displays