Original source

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

Alleles
T/C | Ancestral: C | Ambiguity code: Y | MAF: 0.47 (T)
Location

Chromosome 4:38798089 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM094340

Most severe consequence
Evidence status

Clinical significance

This variation has 3 synonyms - click the plus to show

This variation has 6 HGVS names - click the plus to show

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

Variation displays