Original source

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

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

Chromosome 1:169446450 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM991266

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 12264, 2009_August_001_254_SLC19A2_603941_0004

This variation has 4 HGVS names - click the plus to show

Variation displays