Original source

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

Alleles
T/A | Ancestral: T | Ambiguity code: W | MAF: 0.03 (A)
Location

Chromosome 14:94847262 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM890097

Most severe consequence
Evidence status

Clinical significance

This variation has 5 synonyms - click the plus to show

This variation has 21 HGVS names - click the plus to show

This variation has assays on 4 chips - click the plus to show

Variation displays