Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R
Location

Chromosome 12:122769699 (forward strand) | View in location tab

Most severe consequence
Synonyms

Archive dbSNP rs3185668

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

About this variant

This variant overlaps 7 transcripts and has 1 individual genotype.

Variation displays