Original source

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

Alleles
G/T|Ambiguity code: K|MAF: 0.40 (T)
Location

Chromosome 6:32405921 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

HGVS names

This variant has 6 HGVS names - Hide

6:g.32405921G>T
ENST00000544175.2:c.-229-635C>A
ENST00000446536.2:c.80-638C>A
ENST00000454136.7:c.80-635C>A
ENST00000465865.5:c.80-635C>A
ENST00000374993.4:c.80-635C>A

Genotyping chips

This variant has assays on 13 chips - Show

About this variant

This variant overlaps 5 transcripts, has 4262 sample genotypes, is associated with 3 phenotypes and is mentioned in 8 citations.

Variant displays