Original source

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

Alleles
C/G | Ancestral: C | Ambiguity code: S | MAF: 0.05 (G)
Location

Chromosome 19:44904463 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs661655

HGVS name

19:g.44904463C>G

Genotyping chips

This variation has assays on: Illumina_HumanOmni1-Quad

About this variant

This variant overlaps 12 transcripts, has 2532 individual genotypes and is mentioned in 1 citation.

Variation displays