Original source

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

Alleles
G/A | Ancestral: A | Ambiguity code: R | MAF: 0.01 (A)
Location

Chromosome 10:77974715 (forward strand) | View in location tab

Co-located

with dbSNP rs367810633 (G/-)

Most severe consequence
Evidence status

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

Variation displays