Original source

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

Alleles
C/A/T | Ancestral: C | Ambiguity code: H | MAF: 0.48 (A)
Location

Chromosome 2:210298850 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs117724300, rs61019699

This variant has 10 HGVS names - click the plus to show

About this variant

This variant overlaps 8 transcripts and has 2689 sample genotypes.

Variant displays