Original source

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

Alleles
G/C | Ancestral: T | Ambiguity code: S | MAF: 0.24 (G)
Location

Chromosome 2:232542094 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs57633590

This variant has 3 HGVS names - click the plus to show

About this variant

This variant overlaps 3 transcripts and has 2511 sample genotypes.

Variant displays