Original source

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

Alleles
T/C | Ancestral: T | Ambiguity code: Y | MAF: 0.19 (T)
Location

Chromosome 19:21114093 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs4586578

This variation has 10 HGVS names - click the plus to show

Variation displays