Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R | MAF: 0.11 (A)
Location

Chromosome 10:98367794 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs56495379, rs61199351

HGVS name

10:g.98367794G>A

This variation has assays on 7 chips - click the plus to show

Variation displays