Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|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
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs513974

HGVS names

This variant has 3 HGVS names - Show

About this variant

This variant overlaps 12 transcripts and has 2777 sample genotypes.

Variant displays