Original source

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

Alleles
C/A | Ancestral: C | Ambiguity code: M | MAF: 0.03 (A)
Location

Chromosome 10:6072697 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CR075252

Most severe consequence
Evidence status

Clinical significance

Synonyms

Archive dbSNP rs61839673

HGVS name

10:g.6072697C>A

Genotyping chips

This variation has assays on: Illumina_ImmunoChip

Variation displays