Original source

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

Alleles
C/T|Ancestral: C|Ambiguity code: Y|MAF: 0.21 (T)
Location

Chromosome 6:32396067 (forward strand)|View in location tab

Most severe consequence
 
Synonymous variant
Evidence status

HGVS names

This variant has 8 HGVS names - Hide

6:g.32396067C>T
ENST00000544175.2:c.219G>A
ENST00000544175.2:c.219G>A(p.=)
ENST00000454136.7:c.1050G>A
ENST00000454136.7:c.1050G>A(p.=)
ENST00000465865.5:c.*325G>A
ENST00000374993.4:c.1050G>A
ENST00000374993.4:c.1050G>A(p.=)

Genotyping chips

This variant has assays on 7 chips - Show

About this variant

This variant overlaps 5 transcripts, has 4399 sample genotypes, is associated with 1 phenotype and is mentioned in 12 citations.

Variant displays