Original source

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

Alleles
C/T|Ancestral: C|Ambiguity code: Y|MAF: < 0.01 (T)
Location

Chromosome 11:67490807 (forward strand)|View in location tab

Co-located variant

HGMD-PUBLIC CS083216

Most severe consequence
 
Synonymous variant
Evidence status

Clinical significance

Synonyms

LSDB NM_003977.2:c.807C>T

HGVS names

This variant has 8 HGVS names - Show

About this variant

This variant overlaps 13 transcripts, has 2504 sample genotypes and is associated with 1 phenotype.

Variant displays