Original source

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

Alleles
A/G | Ancestral: G | Ambiguity code: R | MAF: 0.15 (A)
Location

Chromosome 10:64415184 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM033482

Most severe consequence
Evidence status

Clinical significance

This variation has 6 synonyms - click the plus to show

This variation has 8 HGVS names - click the plus to show

This variation has assays on 10 chips - click the plus to show

Variation displays