Original source

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

Alleles
C/G | Ancestral: T | Ambiguity code: S | MAF: 0.26 (G)
Location

Chromosome 5:157059492 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs62381165

HGVS name

5:g.157059492C>G

Variation displays