Original source

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

Alleles
T/C | Ancestral: T | Ambiguity code: Y | MAF: 0.15 (C)
Location

Chromosome 6:135097880 (forward strand) | View in location tab

Co-located
Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs61446782

This variant has 2 HGVS names - click the plus to show

6:g.135097880T>C
ENST00000529882.5:c.88+5048A>G

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

About this variant

This variant overlaps 1 transcript, has 2505 sample genotypes, is associated with 12 phenotypes and is mentioned in 38 citations.

Variant displays