Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R | MAF: 0.29 (A)
Location

Chromosome 10:122461028 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CR065642

Most severe consequence
Evidence status

Clinical significance

HGVS name

10:g.122461028G>A

Genotyping chips

This variation has assays on: Illumina_ExomeChip, HumanCoreExome-12

Variation displays