Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

Alleles
C/G/T|Ancestral: C|Ambiguity code: B|MAF: < 0.01 (T)
Location

Chromosome 1:169477212 (forward strand)|View in location tab

Co-located variant

HGMD-PUBLIC CM991266

Most severe consequence
 
Stop gained
Evidence status

Clinical significance

Synonyms

LSDB 12264, 2009_August_001_254_SLC19A2_603941_0004

HGVS names

This variant has 8 HGVS names - Show

About this variant

This variant overlaps 6 transcripts, has 2504 sample genotypes and is associated with 2 phenotypes.

Variant displays