Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

Alleles
A/G | Ancestral: A | Ambiguity code: R | MAF: 0.43 (G)
Location

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

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs17405275, rs60245055

This variation has 14 HGVS names - click the plus to show

1:g.65579645A>G
ENST00000371059.5:c.494+7196A>G
ENST00000349533.8:c.494+7196A>G
ENST00000616738.2:c.494+7196A>G
ENST00000462765.3:n.644+7196A>G
ENST00000344610.10:c.494+7196A>G
ENST00000406510.5:c.-127+7196A>G
ENST00000371060.5:c.494+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

Variation displays