Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R
Location

Chromosome 1:230837787 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

1:g.230837787G>A

Variation displays