Original source

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

Alleles
G/A | Ancestral: A | Ambiguity code: R | MAF: 0.43 (A)
Location

Chromosome 11:71308366 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs1792204, rs59491796

HGVS name

11:g.71308366G>A

This variation has assays on 13 chips - click the plus to show

Variation displays