Original source

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

Alleles
G/C|Ancestral: G|Ambiguity code: S
Location

Chromosome 15:64156761 (forward strand)|View in location tab

Most severe consequence
 
Synonymous variant
Evidence status

Clinical significance

Synonyms
HGVS names

This variant has 9 HGVS names - Show

About this variant

This variant overlaps 11 transcripts, has 94 sample genotypes and is associated with 1 phenotype.

Variant displays