Original source

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

Alleles
T/G | Ancestral: G | Ambiguity code: K | MAF: 0.23 (G)
Location

Chromosome 20:5316005 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs58194117, rs17721333

HGVS name

20:g.5316005T>G

This variation has assays on 7 chips - click the plus to show

Variation displays