Original source

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

Alleles
T/C|Ancestral: C|Ambiguity code: Y|MAF: 0.29 (T)
Location

Chromosome 9:114790605 (forward strand)|View in location tab

Co-located variants
Most severe consequence
 
Synonymous variant
Evidence status

Synonyms

Archive dbSNP rs59393366

HGVS names

This variant has 5 HGVS names - Hide

9:g.114790605T>C
ENST00000374044.1:c.372A>G
ENST00000374044.1:c.372A>G(p.=)
ENST00000374045.4:c.603A>G
ENST00000374045.4:c.603A>G(p.=)

Genotyping chips

This variant has assays on 9 chips - Show

About this variant

This variant overlaps 2 transcripts, 1 regulatory feature, has 4070 sample genotypes, is associated with 2 phenotypes and is mentioned in 18 citations.

Variant displays