Original source

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

Alleles
A/G | Ancestral: G | Ambiguity code: R | MAF: 0.49 (G)
Location

Chromosome 19:41818506 (forward strand) | View in location tab

Most severe consequence
 
Intergenic variant
Evidence status

Synonyms

Archive dbSNP rs59430921, rs74259553

HGVS name

19:g.41818506A>G

This variant has assays on 6 chips - click the plus to show

About this variant

This variant has 3680 sample genotypes.

Variant displays