Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

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

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

Most severe consequence
Evidence status

Synonyms
HGVS name

19:g.5830436C>T

Genotyping chips

This variation has assays on: Illumina_Human1M-duo

About this variant

This variant overlaps 12 transcripts and has 1192 individual genotypes.

Variation displays