Original source

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

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

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

Co-located variant

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

HGVS names

This variant has 7 HGVS names - Show

About this variant

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

Variant displays