Original source

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

Alleles
C/G | Ancestral: C | Ambiguity code: S | MAF: 0.04 (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 1121 individual genotypes and is mentioned in 1 citation.

Variation displays