Original source

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

Alleles
C/A | Ancestral: C | Ambiguity code: M
Location

Chromosome 3:122284482 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM002582 ; PhenCode CASRdb_c.2528C>A (C/A)

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 9999, 2010_April_001_048_CASR_601199_0034

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

Variation displays