Original source

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

Alleles
A/C | Ancestral: A | Ambiguity code: M | MAF: 0.11 (C)
Location

Chromosome 11:7001129 (forward strand) | View in location tab

Most severe consequence
Evidence status

This variation has 5 synonyms - click the plus to show

This variation has 5 HGVS names - click the plus to show

This variation has assays on 9 chips - click the plus to show

Variation displays