Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
T/C | Ancestral: T | Ambiguity code: Y | MAF: 0.40 (T)
Location

Chromosome 2:231513520 (forward strand) | View in location tab

Most severe consequence
 
Splice region variant
Evidence status

Synonyms

Archive dbSNP rs59272379

This variant has 2 HGVS names - click the plus to show

This variant has assays on 5 chips - click the plus to show

About this variant

This variant overlaps 1 transcript, has 3769 sample genotypes, is associated with 1 phenotype and is mentioned in 1 citation.

Variant displays