Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP

Alleles
C/T | Ambiguity code: Y | MAF: 0.26 (C)
Location

Chromosome 19:21296897 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs4318333

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

Variation displays