Original source

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

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

Chromosome 1:206773289 (forward strand)|View in location tab

Co-located variant

HGMD-PUBLIC CR086313

Most severe consequence
 
Upstream gene variant
Evidence status

Synonyms
HGVS name

1:g.206773289A>G

Genotyping chips

This variant has assays on 8 chips - Show

About this variant

This variant overlaps 3 transcripts, has 3374 sample genotypes, is associated with 1 phenotype and is mentioned in 204 citations.

Variant displays