Original source

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

Alleles
-/G | MAF: 0.47 (G)
Location

Chromosome 11: between 102468779 and 102468780 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs149118200, rs56736408

This variation has 3 HGVS names - click the plus to show

Variation displays