Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|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
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs58177610

HGVS names

This variant has 10 HGVS names - Hide

1:g.50139665T>C
ENST00000463650.1:n.262-5292T>C
ENST00000357083.8:c.118-5292T>C
ENST00000371819.1:c.25-5292T>C
ENST00000371824.5:c.10-5292T>C
ENST00000448907.6:c.19-5292T>C
ENST00000371821.5:c.25-5292T>C
ENST00000371827.5:c.10-5292T>C
ENST00000494555.1:n.150-2107T>C
ENST00000371823.8:c.10-5292T>C

Genotyping chips

This variant has assays on 11 chips - Show

About this variant

This variant overlaps 9 transcripts, has 3765 sample genotypes and is mentioned in 4 citations.

Variant displays