Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | View in dbSNP

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

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

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs10348357

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

7:g.34709170G>C
ENST00000419766.2:n.241+19567C>G
ENST00000359791.2:c.280+24486G>C
ENST00000381544.3:c.280+24486G>C
ENST00000531252.2:c.280+24486G>C
ENST00000431669.2:n.244+19567C>G
ENST00000381539.3:c.280+24486G>C
ENST00000381542.2:c.280+24486G>C
ENST00000381553.4:c.280+24486G>C
ENST00000396095.3:c.280+24486G>C
ENST00000428922.2:n.161-4971C>G
ENST00000439852.2:n.280-4971C>G
ENST00000358772.5:n.279+19567C>G
ENST00000360581.2:c.280+24486G>C
ENST00000539747.2:n.160+19567C>G

Genotyping chips

This variation has assays on: Illumina_HumanOmni5, Illumina_1M-duo

Variation displays