Original source

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

Alleles
T/C|Ambiguity code: Y
Location

Chromosome 6:32641650 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms
HGVS names

This variant has 7 HGVS names - Hide

6:g.32641650T>C
ENST00000374949.2:c.331+92T>C
ENST00000395363.5:c.331+92T>C
ENST00000496318.5:c.331+92T>C
ENST00000482745.5:c.*1163+92T>C
ENST00000460633.1:n.359+92T>C
ENST00000343139.9:c.331+92T>C

Genotyping chips

This variant has assays on: Illumina_Human1M-duo, Affy GenomeWideSNP_6.0, Affy GeneChip 500K

About this variant

This variant overlaps 7 transcripts, has 1379 sample genotypes and is mentioned in 6 citations.

Variant displays