Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | 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

This variant has 4 HGVS names - click the plus to show

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

This variant has assays on 8 chips - click the plus to show

About this variant

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

Variant displays