Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
G/A | Ancestral: G | Ambiguity code: R
Location

Chromosome 2:55037814 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs4319970

This variant has 11 HGVS names - click the plus to show

About this variant

This variant overlaps 10 transcripts and has 1 sample genotype.

Variant displays