Original source

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

A/G/T | Ancestral: A | Ambiguity code: D

Chromosome 11:5246718 (forward strand) | View in location tab


with HGMD-PUBLIC CR014260, CR045224, CR850010 ; PhenCode HbVar.968 (A/G)

Most severe consequence
Evidence status

Clinical significance

This variation has 4 synonyms - click the plus to show

This variation has 4 HGVS names - click the plus to show

Variation displays