Original source

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

Alleles
T/A/C | Ancestral: T | Ambiguity code: H
Location

Chromosome 3:122003218 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM960245 ; PhenCode CASRdb_c.2417T>C (T/C)

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_035_CASR_601199_0011, 9977

This variation has 14 HGVS names - click the plus to show

Variation displays