Original source

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

Alleles
C/G|Ancestral: C|Ambiguity code: S
Location

Chromosome 20:46725279 (forward strand)|View in location tab

Co-located variant

HGMD-PUBLIC CM061196

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

LSDB 13566, 2009_August_001_071_SLC2A10_606145_0004

HGVS names

This variant has 4 HGVS names - Show

About this variant

This variant overlaps 2 transcripts and is associated with 2 phenotypes.

Variant displays