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 1:77088718 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

1:g.77088718C>G

Variation displays