Original source

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

Alleles
G/- | Ancestral: G | MAF: 0.40 (G)
Location

Chromosome 11:47349934 (forward strand) | View in location tab

Co-located

with dbSNP rs181840234 (G/A)

Most severe consequence
Evidence status

Clinical significance

Synonyms

This variation has 7 HGVS names - click the plus to show

Variation displays