Original source

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

Alleles
-/C/CC | Ancestral: G | MAF: 0.38 (C)
Location

Chromosome 11: between 2905204 and 2905205 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs375826791, rs140121791

This variation has 14 HGVS names - click the plus to show

Variation displays