Original source

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

Alleles
T/C | Ancestral: C | Ambiguity code: Y | MAF: < 0.01 (T)
Location

Chromosome 19:19358820 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs61503628

HGVS name

19:g.19358820T>C

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

Variation displays