Original source

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

Alleles
T/C|Ancestral: T|Ambiguity code: Y|MAF: 0.29 (C)
Location

Chromosome 14:103712930 (forward strand)|View in location tab

Co-located variant

HGMD-PUBLIC CR057423

Most severe consequence
 
Splice region variant
Evidence status

Synonyms

Archive dbSNP rs3212034

HGVS names

This variant has 14 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_HumanOmni2.5, Illumina_HumanOmni1-Quad, Illumina_HumanOmni5

About this variant

This variant overlaps 22 transcripts, has 2857 sample genotypes and is mentioned in 22 citations.

Variant displays