Original source

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

Alleles
T/A/C | Ancestral: T | Ambiguity code: H | MAF: 0.31 (C)
Location

Chromosome 11:1995429 (forward strand) | View in location tab

Most severe consequence

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

Evidence status

Synonyms

This variation has 22 HGVS names - click the plus to show

This variation has assays on 4 chips - click the plus to show

Variation displays