Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R | MAF: 0.25 (A)
Location

Chromosome 11:68362138 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs659525, rs57141796

This variation has 3 HGVS names - click the plus to show

This variation has assays on 7 chips - click the plus to show

Variation displays