Original source

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

Alleles
C/T | Ancestral: T | Ambiguity code: Y
Location

Chromosome 19:5830436 (forward strand) | View in location tab

Co-located

with dbSNP rs371327345 (C/-/T)

Most severe consequence
Evidence status

Synonyms
HGVS name

19:g.5830436C>T

Genotyping chips

This variation has assays on: Illumina_1M-duo

Variation displays