Original source

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

Alleles
T/G | Ancestral: T | Ambiguity code: K
Location

Chromosome 9:69072646 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM993649

Most severe consequence
Evidence status

Clinical significance

This variation has 4 synonyms - click the plus to show

This variation has 9 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_Human610_Quad, Illumina_Human1M-duo

Variation displays