Original source

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

Alleles
T/G | Ancestral: T | Ambiguity code: K | MAF: < 0.01 (G)
Location

Chromosome 19:42085760 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

19:g.42085760T>G

Variation displays