Original source

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

Alleles
C/G/T | Ancestral: C | Ambiguity code: B | MAF: < 0.01 (G)
Location

Chromosome 4:121809676 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

LSDB NC_000004.11:g.121809676C>G

This variation has 16 HGVS names - click the plus to show

Variation displays