Original source

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

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

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

Co-located

with HGMD-PUBLIC CM061196

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 13566, 2009_August_001_071_SLC2A10_606145_0004

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

20:g.46725279C>G
ENST00000359271.3:c.243C>G
ENSP00000352216.2:p.Ser81Arg
ENST00000611837.1:n.395C>G

Variation displays