Original source

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

Alleles
T/C | Ancestral: T | Ambiguity code: Y | MAF: 0.02 (C)
Location

Chromosome 16:23634833 (forward strand) | View in location tab

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB NM_024675.3:c.1684+29A>G

This variation has 6 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_HumanOmni5

Variation displays