Original source

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

Alleles
G/T | Ancestral: T | Ambiguity code: K | MAF: < 0.01 (G)
Location

Chromosome 16:31188078 (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 rs60903675

This variation has 7 HGVS names - click the plus to show

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

Variation displays