Original source

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

Alleles
C/T|Ancestral: T|Ambiguity code: Y|MAF: 0.44 (T)
Location

Chromosome 4:167115073 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs56847147, rs386615660

HGVS names

This variant has 26 HGVS names - Show

Genotyping chips

This variant has assays on 9 chips - Show

About this variant

This variant overlaps 25 transcripts, has 3759 sample genotypes and is associated with 1 phenotype.

Variant displays