Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | View in dbSNP

Alleles
A/G | Ancestral: A | Ambiguity code: R | MAF: 0.30 (A)
Location

Chromosome 16:88646828 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM983302

Most severe consequence
Evidence status

Clinical significance

This variation has 10 synonyms - click the plus to show

This variation has 17 HGVS names - click the plus to show

This variation has assays on 10 chips - click the plus to show

Variation displays