Original source

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

Alleles
G/C|Ancestral: C|Ambiguity code: S|MAF: 0.39 (C)
Location

Chromosome 9:133643810 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs59265623

HGVS names

This variant has 2 HGVS names - Hide

9:g.133643810G>C
ENST00000393056.6:c.921+221G>C

About this variant

This variant overlaps 2 transcripts, has 2781 sample genotypes and is mentioned in 2 citations.

Variant displays