Original source

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

C/T | Ancestral: C | Ambiguity code: Y

Chromosome 14:94849160 (forward strand) | View in location tab


with HGMD-PUBLIC CM900183

Most severe consequence
Evidence status

Clinical significance

This variation has 3 synonyms - click the plus to show

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

Variation displays