Original source

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

Alleles
C/G | Ancestral: G | Ambiguity code: S | MAF: 0.36 (C)
Location

Chromosome 20:41005726 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms
HGVS name

20:g.41005726C>G

Genotyping chips

This variation has assays on: Affy GenomeWideSNP_6.0

Variation displays