Original source

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

Alleles
T/C | Ancestral: C | Ambiguity code: Y | MAF: 0.43 (C)
Location

Chromosome 16:3304654 (forward strand) | View in location tab

Most severe consequence
Evidence status

Clinical significance

This variation has 3 synonyms - click the plus to show

This variation has 16 HGVS names - click the plus to show

Variation displays