Original source

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

Alleles
A/G|Ancestral: A|Ambiguity code: R|MAF: 0.37 (G)
Location

Chromosome 1:65579645 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs17405275, rs60245055

HGVS names

This variant has 14 HGVS names - Hide

1:g.65579645A>G
ENST00000371059.7:c.494+7196A>G
ENST00000349533.10:c.494+7196A>G
ENST00000616738.4:c.494+7196A>G
ENST00000344610.12:c.494+7196A>G
ENST00000462765.5:n.644+7196A>G
ENST00000371060.7:c.494+7196A>G
ENST00000406510.7:c.-127+7196A>G
ENST00000371058.1:c.494+7196A>G
LRG_283:g.164081A>G
LRG_283t2:c.494+7196A>G
LRG_283t3:c.494+7196A>G
LRG_283t4:c.494+7196A>G
LRG_283t1:c.494+7196A>G

About this variant

This variant overlaps 13 transcripts, has 4936 sample genotypes and is mentioned in 1 citation.

Variant displays