Original source

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

Alleles
A/G | Ancestral: A | Ambiguity code: R | MAF: 0.06 (G)
Location

Chromosome 10:31429519 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs172849, rs56692821

This variation has 25 HGVS names - click the plus to show

Variation displays