Original source

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

Alleles
T/C | Ancestral: C | Ambiguity code: Y | MAF: 0.48 (C)
Location

Chromosome 1:50139665 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs58177610

This variation has 10 HGVS names - click the plus to show

1:g.50139665T>C
ENST00000463650.1:n.262-5292T>C
ENST00000357083.5:c.61-5292T>C
ENST00000371819.1:c.25-5292T>C
ENST00000371824.2:c.10-5292T>C
ENST00000448907.3:c.19-5292T>C
ENST00000371821.2:c.25-5292T>C
ENST00000371827.2:c.10-5292T>C
ENST00000494555.1:n.150-2107T>C
ENST00000371823.5:c.10-5292T>C

This variation has assays on 10 chips - click the plus to show

Variation displays