Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R | MAF: 0.38 (A)
Location

Chromosome 9:78548557 (forward strand) | View in location tab

Most severe consequence
 
Intergenic variant
Evidence status

Synonyms

Archive dbSNP rs61616381

HGVS name

9:g.78548557G>A

This variant has assays on 7 chips - click the plus to show

About this variant

This variant has 3989 sample genotypes and is mentioned in 1 citation.

Variant displays