Original source

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

Alleles
C/A/T|Ancestral: C|Ambiguity code: H|MAF: 0.02 (T)
Location

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

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs117724300, rs61019699

HGVS names

This variant has 10 HGVS names - Show

About this variant

This variant overlaps 8 transcripts and has 2689 sample genotypes.

Variant displays