Original source

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

Alleles
T/G | Ancestral: T | Ambiguity code: K
Location

Chromosome 20:938859 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

20:g.938859T>G

Variation displays