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 15:73929861 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs56431870, rs57313558

HGVS names

This variant has 3 HGVS names - Hide

15:g.73929861T>C
ENST00000566011.5:c.1102+1976T>C
ENST00000261921.7:c.1102+1976T>C

Genotyping chips

This variant has assays on 10 chips - Show

About this variant

This variant overlaps 14 transcripts, has 3696 sample genotypes, is associated with 2 phenotypes and is mentioned in 54 citations.

Variant displays