Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | 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

This variant has 5 HGVS names - click the plus to show

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

This variant has assays on 12 chips - click the plus to show

About this variant

This variant overlaps 5 transcripts, 1 regulatory feature, has 4576 sample genotypes and is mentioned in 1 citation.

Variant displays