Original source

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

Alleles
G/C | Ancestral: G | Ambiguity code: S | MAF: 0.41 (C)
Location

Chromosome 16:3144656 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs513974

This variation has 4 HGVS names - click the plus to show

About this variant

This variant overlaps 12 transcripts and has 2777 individual genotypes.

Variation displays