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 3:122283896 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM010178 ; PhenCode CASRdb_c.1942C>T (C/T)

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 9997, 2010_April_001_047_CASR_601199_0032

This variation has 5 HGVS names - click the plus to show

Variation displays