Original source

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

C/T | Ambiguity code: Y | MAF: 0.11 (T)

Chromosome 6:31306778 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status

HGVS names

This variant has 2 HGVS names - Hide


Genotyping chips

This variant has assays on 13 chips - Show

About this variant

This variant overlaps 2 transcripts, has 5658 sample genotypes, is associated with 3 phenotypes and is mentioned in 26 citations.

Variant displays