Original source

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

Alleles
C/T|Ancestral: C|Ambiguity code: Y
Location

Chromosome 12:6845711 (forward strand)|View in location tab

Co-located variant

HGMD-PUBLIC CS983412

Most severe consequence
 
Synonymous variant
Evidence status

Synonyms
HGVS names

This variant has 12 HGVS names - Show

Genotyping chips

This variant has assays on 5 chips - Show

About this variant

This variant overlaps 21 transcripts, has 2880 sample genotypes and is mentioned in 52 citations.

Variant displays