Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

Alleles
C/A|Ancestral: C|Ambiguity code: M|MAF: 0.45 (C)
Location

Chromosome 5:136041660 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs60080137, rs56429354

HGVS names

This variant has 5 HGVS names - Hide

5:g.136041660C>A
ENST00000504185.5:n.302-2398C>A
ENST00000506699.5:n.299-2398C>A
ENST00000442011.6:c.234-2398C>A
ENST00000507018.5:c.151-2398C>A

Genotyping chips

This variant has assays on 12 chips - Show

About this variant

This variant overlaps 5 transcripts, 1 regulatory feature, has 5942 sample genotypes and is mentioned in 1 citation.

Variant displays