Original source

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

Alleles
G/C | Ancestral: G | Ambiguity code: S | MAF: 0.28 (G)
Location

Chromosome 12:11686714 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs79747998, rs1210185, rs862791

This variation has 6 HGVS names - click the plus to show

About this variant

This variant overlaps 4 transcripts and has 1105 individual genotypes.

Variation displays