Original source

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

Alleles
T/C|Ancestral: C|Ambiguity code: Y|MAF: 0.41 (T)
Location

Chromosome 14:33241581 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs386567094

HGVS names

This variant has 11 HGVS names - Hide

14:g.33241581T>C
ENST00000549770.1:n.245+26155T>C
ENST00000551492.5:c.406+26155T>C
ENST00000548645.5:c.295+26155T>C
ENST00000357798.9:c.346+25994T>C
ENST00000356141.8:c.385+26155T>C
ENST00000546849.1:c.115+26155T>C
ENST00000551008.5:c.79+26155T>C
ENST00000547068.5:c.79+26155T>C
ENST00000551634.5:c.316+26155T>C
ENST00000346562.6:c.295+26155T>C

Genotyping chips

This variant has assays on 5 chips - Show

About this variant

This variant overlaps 10 transcripts and has 5801 sample genotypes.

Variant displays