Original source

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

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

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

Most severe consequence
 
Downstream gene variant
Evidence status

HGVS name

6:g.31306778C>T

Genotyping chips

This variant has assays on 13 chips - Show

About this variant

This variant overlaps 1 transcript, has 5658 sample genotypes, is associated with 3 phenotypes and is mentioned in 26 citations.

Variant displays