Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
C/A | Ancestral: C | Ambiguity code: M
Location

Chromosome 11:67365224 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM066008

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

LSDB 15152, 2010_April_001_029_CLCF1_607672_0002, NM_013246.2:c.590G>T

This variant has 7 HGVS names - click the plus to show

About this variant

This variant overlaps 5 transcripts and is associated with 2 phenotypes.

Variant displays