Original source

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

Alleles
G/A|Ancestral: A|Ambiguity code: R|MAF: 0.26 (A)
Location

Chromosome 10:81896770 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs57146204

HGVS names

This variant has 8 HGVS names - Hide

10:g.81896770G>A
ENST00000555784.5:c.135+18675G>A
ENST00000602794.5:c.*371+7105G>A
ENST00000404547.5:c.823+20607G>A
ENST00000404576.6:c.135+18675G>A
ENST00000556918.5:c.135+18675G>A
ENST00000372142.6:c.60+18750G>A
ENST00000372141.6:c.823+20607G>A

Genotyping chips

This variant has assays on 10 chips - Show

About this variant

This variant overlaps 7 transcripts, has 3963 sample genotypes and is mentioned in 4 citations.

Variant displays