Original source

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

Alleles
-/C
Location

Chromosome 11: between 5225720 and 5225721 (forward strand) | View in location tab

Most severe consequence
Evidence status

Clinical significance

Synonyms

HbVar 945

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

Variation displays