Original source

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

Alleles
C/T|Ancestral: T|Ambiguity code: Y|MAF: 0.01 (C)
Location

Chromosome 2:203874002 (forward strand)|View in location tab

Most severe consequence
 
Downstream gene variant
Evidence status

Synonyms
HGVS name

2:g.203874002C>T

Genotyping chips

This variant has assays on 4 chips - Show

About this variant

This variant overlaps 5 transcripts, has 3550 sample genotypes and is mentioned in 1 citation.

Variant displays