Original source

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

Alleles
G/C | Ancestral: C | Ambiguity code: S | MAF: 0.17 (C)
Location

Chromosome 6:52419923 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs3761989

HGVS name

6:g.52419923G>C

Variation displays