Original source

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

Alleles
G/C|Ancestral: C|Ambiguity code: S
Location

Chromosome 2:46302120 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs59977781

HGVS names

This variant has 5 HGVS names - Show

About this variant

This variant overlaps 4 transcripts and has 4 sample genotypes.

Variant displays