Original source

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

Alleles
C/T | Ancestral: T | Ambiguity code: Y | MAF: 0.40 (C)
Location

Chromosome 2:48962782 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM052876

Most severe consequence
Evidence status

Clinical significance

This variation has 8 synonyms - click the plus to show

This variation has 5 HGVS names - click the plus to show

This variation has assays on 13 chips - click the plus to show

Variation displays