Original source

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

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

Chromosome 10:100127551 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs56495379, rs61199351

HGVS name

10:g.100127551G>A

This variation has assays on 5 chips - click the plus to show

Variation displays