Original source

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

Alleles
G/T | Ancestral: G | Ambiguity code: K | MAF: 0.15 (T)
Location

Chromosome 4:53378156 (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 rs61522860, rs3811784

This variation has 9 HGVS names - click the plus to show

Variation displays