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
ENST00000419766.3:n.241+19567C>G
ENST00000359791.3:c.280+24486G>C
ENST00000381544.4:c.280+24486G>C
ENST00000531252.3:c.280+24486G>C
ENST00000431669.3:n.244+19567C>G
ENST00000381539.3:c.280+24486G>C
ENST00000381542.3:c.280+24486G>C
ENST00000396095.4:c.280+24486G>C
ENST00000381553.5:c.280+24486G>C
ENST00000439852.3:n.280-4971C>G
ENST00000428922.3:n.161-4971C>G
ENST00000358772.6:n.279+19567C>G
ENST00000539747.3:n.160+19567C>G
ENST00000360581.3:c.280+24486G>C

Genotyping chips

This variation has assays on: Illumina_HumanOmni5, Illumina_Human1M-duo

Variation displays