Original source

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

Alleles
C/G|Ancestral: C|Ambiguity code: S|MAF: 0.11 (G)
Location

Chromosome 4:89772325 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs17796079

HGVS names

This variant has 12 HGVS names - Show

About this variant

This variant overlaps 11 transcripts, has 3116 sample genotypes and is mentioned in 2 citations.

Variant displays