Original source

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

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

Chromosome 1:169468793 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM002429

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 2009_August_001_255_SLC19A2_603941_0009, 12269

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

Variation displays