Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

G/C | Ancestral: G | Ambiguity code: S | MAF: 0.49 (G)

Chromosome 13:75587064 (forward strand) | View in location tab

Most severe consequence
Evidence status


Archive dbSNP rs12866981, rs58838644

This variation has 8 HGVS names - click the plus to show

About this variant

This variant overlaps 7 transcripts and has 1358 individual genotypes.

Variation displays