Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | View in dbSNP

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

Chromosome 3:122284134 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM062491 ; PhenCode CASRdb_c.2180T>A (T/A)

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 10010, 2010_April_001_058_CASR_601199_0045

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

Variation displays