Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
G/A/C | Ancestral: C | Ambiguity code: V | MAF: 0.12 (G)
Location

Chromosome 19:17403631 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs12975139

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

About this variant

This variant overlaps 40 transcripts and has 2776 individual genotypes.

Variation displays