Original source

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

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

Chromosome 9:97678875 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs368692213, rs138496582

This variation has 5 HGVS names - click the plus to show

Variation displays