Original source

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

Synonyms

Archive dbSNP rs61446782

HGVS names

This variant has 2 HGVS names - Hide

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

Genotyping chips

This variant has assays on 10 chips - Show

About this variant

This variant overlaps 1 transcript, has 3681 sample genotypes, is associated with 12 phenotypes and is mentioned in 42 citations.

Variant displays