Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

Alleles
C/G/T | Ancestral: C | Ambiguity code: B | MAF: < 0.01 (G)
Location

Chromosome 17:50170245 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM971346 ; PhenCode SGCA:c.850C>T (C/T)

Most severe consequence
Evidence status

Clinical significance

This variation has 2 synonyms - click the plus to show

This variation has 26 HGVS names - click the plus to show

Variation displays