Original source

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

C/A | Ancestral: C | Ambiguity code: M

Chromosome 2:236167390 (forward strand) | View in location tab

Most severe consequence
Intron variant
HGVS names

This variant has 3 HGVS names - Show

About this variant

This variant overlaps 5 transcripts and 1 regulatory feature.

Variant displays