Original source

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

Alleles
G/A|Ancestral: G|Ambiguity code: R|MAF: 0.44 (A)
Location

Chromosome 13:46895805 (forward strand)|View in location tab

Co-located variant

HGMD-PUBLIC CM960851

Most severe consequence
 
Synonymous variant
Evidence status

Synonyms
HGVS names

This variant has 8 HGVS names - Show

Genotyping chips

This variant has assays on 12 chips - Show

About this variant

This variant overlaps 4 transcripts, has 4438 sample genotypes and is mentioned in 99 citations.

Variant displays