Original source

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

Alleles
C/-|Ancestral: C
Location

Chromosome 2:232543488 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs377643922

HGVS names

This variant has 3 HGVS names - Show

About this variant

This variant overlaps 4 transcripts.

Variant displays