Original source

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

Alleles
G/A|Ancestral: A|Ambiguity code: R|MAF: 0.43 (A)
Location

Chromosome 19:46225962 (forward strand)|View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

Synonyms

Archive dbSNP rs58273978, rs17660257

HGVS name

19:g.46225962G>A

About this variant

This variant overlaps 2 transcripts and has 2850 sample genotypes.

Variant displays