Original source

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

Alleles
G/A|Ancestral: G|Ambiguity code: R|MAF: 0.10 (A)
Location

Chromosome 9:104885374 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs60254778

HGVS names

This variant has 4 HGVS names - Hide

9:g.104885374G>A
ENST00000374733.1:c.-20-806C>T
ENST00000374736.7:c.161-806C>T
ENST00000423487.6:c.161-806C>T

Genotyping chips

This variant has assays on 10 chips - Show

About this variant

This variant overlaps 3 transcripts, has 3967 sample genotypes, is associated with 5 phenotypes and is mentioned in 22 citations.

Variant displays