Original source

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

Alleles
C/T|Ancestral: T|Ambiguity code: Y|MAF: 0.27 (C)
Location

Chromosome 2:55865477 (forward strand)|View in location tab

Most severe consequence
 
Downstream gene variant
Evidence status

Synonyms
HGVS name

2:g.55865477C>T

Genotyping chips

This variant has assays on 11 chips - Show

About this variant

This variant overlaps 4 transcripts, 1 regulatory feature, has 4418 sample genotypes and is mentioned in 1 citation.

Variant displays