Original source

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

Alleles
G/C | Ancestral: C | Ambiguity code: S | MAF: 0.23 (C)
Location

Chromosome 20:5315842 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs17721327

HGVS name

20:g.5315842G>C

This variation has assays on 4 chips - click the plus to show

Variation displays