Original source

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

Alleles
C/G | Ancestral: G | Ambiguity code: S | MAF: 0.19 (G)
Location

Chromosome 9:75769950 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs61137487

This variation has 5 HGVS names - click the plus to show

Variation displays