Original source

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

Alleles
A/G | Ancestral: A | Ambiguity code: R | MAF: 0.39 (G)
Location

Chromosome 11:66053202 (forward strand) | View in location tab

Most severe consequence

 
Non coding transcript exon variant
| See all predicted consequences [Genes and regulation]

Evidence status

Synonyms

Archive dbSNP rs61232781

This variation has 11 HGVS names - click the plus to show

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

Variation displays