Original source

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

Alleles
A/G|Ancestral: G|Ambiguity code: R|MAF: 0.41 (A)
Location

Chromosome 1:206770888 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs386537477, rs61317010

HGVS names

This variant has 4 HGVS names - Hide

1:g.206770888A>G
ENST00000367099.3:n.283+19T>C
ENST00000471071.1:n.293+19T>C
ENST00000423557.1:c.378+19T>C

Genotyping chips

This variant has assays on 8 chips - Show

About this variant

This variant overlaps 3 transcripts, 1 regulatory feature, has 4676 sample genotypes and is mentioned in 35 citations.

Variant displays