Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP

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

Chromosome 1:66045328 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs17405275, rs60245055

This variation has 13 HGVS names - click the plus to show

1:g.66045328A>G
ENST00000371059.3:c.494+7196A>G
ENST00000349533.6:c.494+7196A>G
ENST00000344610.8:c.494+7196A>G
ENST00000462765.1:n.644+7196A>G
ENST00000371060.3:c.494+7196A>G
ENST00000406510.3:c.-127+7196A>G
ENST00000371058.1:c.494+7196A>G
LRG_283:g.164081A>G
LRG_283t2.1:c.494+7196A>G
LRG_283t3.1:c.494+7196A>G
LRG_283t4.1:c.494+7196A>G
LRG_283t1.1:c.494+7196A>G

Variation displays