This variation has been flagged

Variation has more than 3 different alleles

Original source

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

Alleles
G/A/C/T | Ancestral: G | Ambiguity code: N | MAF: < 0.01 (C)
Location

Chromosome 11:34916134 (forward strand) | View in location tab

Most severe consequence
Evidence status

This variation has 15 HGVS names - click the plus to show

Variation displays