Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP

Alleles
G/C | Ancestral: C | Ambiguity code: S | MAF: 0.47 (C)
Location

Chromosome 7:34748782 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs10348357

This variation has 18 HGVS names - click the plus to show

7:g.34748782G>C
ENST00000381544.2:c.280+24486G>C
ENST00000535640.1:n.244+19567C>G
ENST00000381539.3:c.280+24486G>C
ENST00000381553.3:c.280+24486G>C
ENST00000360581.1:c.280+24486G>C
ENST00000358772.4:n.279+19567C>G
ENST00000419766.1:n.160+19567C>G
ENST00000359791.1:c.280+24486G>C
ENST00000537560.1:n.279+19567C>G
ENST00000544556.1:n.279+19567C>G
ENST00000531252.1:c.280+24486G>C
ENST00000431669.1:n.244+19567C>G
ENST00000396095.2:c.280+24486G>C
ENST00000381542.1:c.280+24486G>C
ENST00000428922.1:n.161-4971C>G
ENST00000439852.1:n.280-4971C>G
ENST00000539747.1:n.164+19567C>G

Genotyping chips

This variation has assays on: Illumina_1M-duo, Illumina_HumanOmni5

Variation displays