Original source

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

Alleles
T/A | Ancestral: T | Ambiguity code: W | MAF: 0.16 (A)
Location

Chromosome 10:6080046 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CR075253

Most severe consequence
Evidence status

Clinical significance

Synonyms

Archive dbSNP rs56584268

HGVS name

10:g.6080046T>A

This variation has assays on 9 chips - click the plus to show

Variation displays