Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.13 (T)
Location

Chromosome 14:94849201 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM900182

Most severe consequence
Evidence status

Clinical significance

This variation has 7 synonyms - click the plus to show

This variation has 27 HGVS names - click the plus to show

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

Variation displays