Original source

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

Alleles
G/- | Ancestral: G | MAF: 0.01 (-)
Location

Chromosome 1:230702566 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

This variation has 2 HGVS names - click the plus to show

Variation displays