Original source

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

Alleles
A/T | Ancestral: A | Ambiguity code: W | MAF: 0.18 (T)
Location

Chromosome 19:44905307 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CR982406 ; dbSNP rs1799820 (A/T)

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs665261, rs1081104

HGVS name

19:g.44905307A>T

Genotyping chips

This variation has assays on: Illumina_Cardio-Metabo_Chip

Variation displays