Original source

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

C/- | Ancestral: C

Chromosome 11:5227018 (forward strand) | View in location tab


with HGMD-PUBLIC CD951722, CM066572, CM973761 ; PhenCode HbVar.218 (C/A), HbVar.713 (C/T), HbVar.781 (C/-) ; dbSNP rs33958358 (C/A/T)

Most severe consequence
Evidence status

Clinical significance

This variation has 2 synonyms - click the plus to show

This variation has 6 HGVS names - click the plus to show

Variation displays