Original source

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

Alleles
T/C|Ancestral: C|Ambiguity code: Y|MAF: 0.24 (T)
Location

Chromosome 7:155461450 (forward strand)|View in location tab

Co-located variant

HGMD-PUBLIC CS045644

Most severe consequence
 
Intron variant
Evidence status

Clinical significance

Synonyms

Archive dbSNP rs3808333

HGVS names

This variant has 2 HGVS names - Hide

7:g.155461450T>C
ENST00000297375.4:c.686-921T>C

Genotyping chips

This variant has assays on 5 chips - Show

About this variant

This variant overlaps 2 transcripts, has 3520 sample genotypes, is associated with 3 phenotypes and is mentioned in 13 citations.

Variant displays