Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

Alleles
G/C|Ancestral: C|Ambiguity code: S|MAF: 0.01 (G)
Location

Chromosome 16:74748216 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs690326

HGVS names

This variant has 3 HGVS names - Show

About this variant

This variant overlaps 2 transcripts and has 2512 sample genotypes.

Variant displays