Original source

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

Alleles
A/G | Ancestral: A | Ambiguity code: R
Location

Chromosome 11:5225705 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM073120, CD991744 ; PhenCode HbVar.488 (A/G)

Most severe consequence
Evidence status

Clinical significance

This variation has 2 synonyms - click the plus to show

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

Variation displays