Original source

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

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

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

Co-located

with HGMD-PUBLIC CR086313

Most severe consequence
Evidence status

Synonyms
HGVS name

1:g.206773289A>G

This variation has assays on 8 chips - click the plus to show

About this variant

This variant overlaps 3 transcripts, has 3374 individual genotypes, is associated with 1 phenotype and is mentioned in 177 citations.

Variation displays