Original source

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

Alleles
A/G | Ancestral: A | Ambiguity code: R | MAF: 0.50 (G)
Location

Chromosome 16:89835097 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs17233092, rs58404229

This variation has 6 HGVS names - click the plus to show

Variation displays