Original source

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

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

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

Most severe consequence
Intron variant
Evidence status


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