Original source

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

Alleles
T/C | Ancestral: T | Ambiguity code: Y
Location

Chromosome 3:122284595 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM001067 ; PhenCode CASRdb_c.2641T>C (T/C)

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_046_CASR_601199_0031, 9996

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

Variation displays