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: 0.06 (C)
Location

Chromosome 19:44905371 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CR984705

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs1799819

HGVS name

19:g.44905371T>C

Genotyping chips

This variation has assays on: Illumina_Cardio-Metabo_Chip

Variation displays