Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.26 (T)
Location

Chromosome 2:17933665 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CR052973

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs386512110

This variant has 2 HGVS names - click the plus to show

2:g.17933665C>T
ENST00000465292.5:n.305+15794C>T

Genotyping chips

This variant has assays on: Illumina_Human1M-duo, Illumina_HumanHap650Y

About this variant

This variant overlaps 4 transcripts, has 3690 sample genotypes and is mentioned in 1 citation.

Variant displays