Original source

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

Alleles
G/C | Ancestral: C | Ambiguity code: S | MAF: 0.46 (C)
Location

Chromosome 7:34709170 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs10348357

This variant has 15 HGVS names - click the plus to show

7:g.34709170G>C
ENST00000419766.5:n.241+19567C>G
ENST00000359791.5:c.280+24486G>C
ENST00000381544.6:c.280+24486G>C
ENST00000531252.5:c.280+24486G>C
ENST00000431669.5:n.244+19567C>G
ENST00000381539.3:c.280+24486G>C
ENST00000381553.7:c.280+24486G>C
ENST00000381542.5:c.280+24486G>C
ENST00000396095.6:c.280+24486G>C
ENST00000428922.5:n.161-4971C>G
ENST00000439852.5:n.280-4971C>G
ENST00000360581.5:c.280+24486G>C
ENST00000358772.8:n.279+19567C>G
ENST00000539747.5:n.160+19567C>G

Genotyping chips

This variant has assays on: Illumina_Human1M-duo, Illumina_HumanOmni5

About this variant

This variant overlaps 15 transcripts, has 2547 sample genotypes and is mentioned in 9 citations.

Variant displays