Original source

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

Alleles
A/G | Ancestral: G | Ambiguity code: R | MAF: 0.33 (G)
Location

Chromosome 9:99150189 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CR102176

Most severe consequence
Evidence status

This variation has 4 HGVS names - click the plus to show

This variation has assays on 5 chips - click the plus to show

About this variant

This variant overlaps 6 transcripts, has 3901 individual genotypes and is mentioned in 15 citations.

Variation displays