Original source

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

Alleles
C/G | Ancestral: C | Ambiguity code: S | MAF: < 0.01 (G)
Location

Chromosome 19:52188362 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

19:g.52188362C>G

Variation displays