Original source

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

Alleles
C/G|Ancestral: G|Ambiguity code: S|MAF: 0.44 (C)
Location

Chromosome 16:88644425 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms
HGVS names

This variant has 7 HGVS names - Show

About this variant

This variant overlaps 13 transcripts and has 3205 sample genotypes.

Variant displays