Original source

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

Alleles
T/C|Ambiguity code: Y|MAF: 0.26 (C)
Location

Chromosome 6:32400310 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms
HGVS names

This variant has 5 HGVS names - Hide

6:g.32400310T>C
ENST00000544175.2:c.-102+1475A>G
ENST00000454136.7:c.730+1475A>G
ENST00000465865.5:c.*5+1475A>G
ENST00000374993.4:c.730+1475A>G

Genotyping chips

This variant has assays on 12 chips - Show

About this variant

This variant overlaps 5 transcripts, has 3690 sample genotypes, is associated with 4 phenotypes and is mentioned in 8 citations.

Variant displays