Original source

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

Alleles
C/T|Ancestral: T|Ambiguity code: Y|MAF: 0.40 (C)
Location

Chromosome 4:88965146 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs61274991, rs17765978

HGVS names

This variant has 6 HGVS names - Hide

4:g.88965146C>T
ENST00000511976.5:c.-22-26905G>A
ENST00000509094.5:c.605+25827G>A
ENST00000512339.5:c.428-26905G>A
ENST00000264344.9:c.605+25827G>A
ENST00000502459.5:n.1063+25827G>A

Genotyping chips

This variant has assays on 10 chips - Show

About this variant

This variant overlaps 5 transcripts, 2 regulatory features, has 3761 sample genotypes and is mentioned in 6 citations.

Variant displays