Original source

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

This variant has 7 HGVS names - click the plus to show

About this variant

This variant overlaps 13 transcripts and has 3205 sample genotypes.

Variant displays