Original source

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

Alleles
T/C|Ancestral: C|Ambiguity code: Y|MAF: 0.22 (T)
Location

Chromosome 6:20728500 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs60110599

HGVS names

This variant has 3 HGVS names - Hide

6:g.20728500T>C
ENST00000274695.8:c.372-11019T>C
ENST00000378610.1:c.372-11019T>C

Genotyping chips

This variant has assays on 15 chips - Show

About this variant

This variant overlaps 3 transcripts, has 4034 sample genotypes, is associated with 3 phenotypes and is mentioned in 33 citations.

Variant displays