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 1:236717896 (forward strand)|View in location tab

Co-located variant

COSMIC COSM4029838

Most severe consequence
 
Synonymous variant
Evidence status

Clinical significance

Synonyms

LSDB ACTN2_165C_T_090710

HGVS names

This variant has 7 HGVS names - Show

About this variant

This variant overlaps 4 transcripts, has 2504 sample genotypes and is associated with 2 phenotypes.

Variant displays