Original source

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

Alleles
C/G/T|Ancestral: C|Ambiguity code: B
Location

Chromosome 11:67490910 (forward strand)|View in location tab

Co-located variant

HGMD-PUBLIC CM061635

Most severe consequence
 
Stop gained
Evidence status

Clinical significance

Synonyms

LSDB NM_003977.2:c.910C>T, 2010_April_001_003_AIP_605555_0003, 13279

HGVS names

This variant has 12 HGVS names - Show

About this variant

This variant overlaps 26 transcripts and is associated with 2 phenotypes.

Variant displays