Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | 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

This variant has 3 HGVS names - click the plus to show

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

This variant has assays on 10 chips - click the plus to show

About this variant

This variant overlaps 14 transcripts, has 3696 sample genotypes, is associated with 2 phenotypes and is mentioned in 52 citations.

Variant displays