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 13:20222992 (forward strand)|View in location tab

Most severe consequence
 
Synonymous variant
Evidence status

Clinical significance

Synonyms

LSDB 11612871

HGVS names

This variant has 9 HGVS names - Show

About this variant

This variant overlaps 4 transcripts, has 2543 sample genotypes and is associated with 2 phenotypes.

Variant displays