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
Location

Chromosome 1:38043485 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

1:g.38043485T>G

Variation displays