Original source

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

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

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

Most severe consequence
Synonymous variant
Evidence status

Clinical significance

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