Original source

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

HGVS names

This variant has 2 HGVS names - Show

Genotyping chips

This variant has assays on 5 chips - 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