Original source

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

Alleles
C/T | Ambiguity code: Y | MAF: 0.08 (T)
Location

Chromosome 19:14730109 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs57246186

This variation has 5 HGVS names - click the plus to show

This variation has assays on 8 chips - click the plus to show

Variation displays