Original source

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

C/G/T | Ancestral: C | Ambiguity code: B

Chromosome 17:15142908 (forward strand) | View in location tab


with HGMD-PUBLIC CM991059, CM031329 ; PhenCode IPNMDB_364 (C/T), IPNMDB_9 (C/G)

Most severe consequence
Evidence status

Clinical significance

This variation has 6 synonyms - click the plus to show

This variation has 32 HGVS names - click the plus to show

Variation displays