Original source

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

Alleles
C/G | Ancestral: C | Ambiguity code: S
Location

Chromosome 5:86563554 (forward strand) | View in location tab

Most severe consequence
HGVS name

5:g.86563554C>G

Variation displays