Original source

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

Alleles
G/A | Ancestral: A | Ambiguity code: R | MAF: 0.25 (A)
Location

Chromosome 10:101861435 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs56552070, rs58359063

HGVS name

10:g.101861435G>A

This variation has assays on 8 chips - click the plus to show

Variation displays