Original source

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

Alleles
A/G|Ancestral: A|Ambiguity code: R|MAF: 0.28 (A)
Location

Chromosome 1:48509774 (forward strand)|View in location tab

Co-located variant

dbSNP rs764850271 (A/-)

Most severe consequence
 
Intergenic variant
Evidence status

Synonyms
HGVS name

1:g.48509774A>G

Genotyping chips

This variant has assays on: Affy GenomeWideSNP_6.0, Affy GeneChip 500K

About this variant

This variant has 5846 sample genotypes.

Variant displays