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 13:48261222 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM991258

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_055_ITM2B_603904_0001, 12245

This variation has 7 HGVS names - click the plus to show

Variation displays