Original source

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

Alleles
G/C/T | Ancestral: G | Ambiguity code: B | MAF: < 0.01 (C)
Location

Chromosome 17:41267809 (forward strand) | View in location tab

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB U14680.1:c.81-13C>G, U14680.1:c.81-13C>A

This variation has 56 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_HumanOmni5

Variation displays