Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | 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 11 HGVS names - click the plus to show

1:g.50139665T>C
ENST00000463650.1:n.262-5292T>C
ENST00000357083.7:c.118-5292T>C
ENST00000371819.1:c.25-5292T>C
ENST00000371824.4:c.10-5292T>C
ENST00000448907.5:c.19-5292T>C
ENST00000371821.4:c.25-5292T>C
ENST00000371827.4:c.10-5292T>C
ENST00000494555.1:n.150-2107T>C
ENST00000625794.1:c.61-5292T>C
ENST00000371823.7:c.10-5292T>C

This variation has assays on 11 chips - click the plus to show

About this variant

This variant overlaps 10 transcripts, has 3765 individual genotypes and is mentioned in 4 citations.

Variation displays