Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R | MAF: 0.49 (A)
Location

Chromosome 19:5830291 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms
HGVS name

19:g.5830291G>A

This variation has assays on 8 chips - click the plus to show

About this variant

This variant overlaps 12 transcripts and has 4311 individual genotypes.

Variation displays