Original source

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

Alleles
A/T | Ancestral: A | Ambiguity code: W | MAF: 0.43 (T)
Location

Chromosome 17:63525082 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

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

17:g.63525082A>T
ENST00000307078.5:c.*1012T>A
LRG_296:g.37659T>A
LRG_296t1.1:c.*1012T>A

This variation has assays on 6 chips - click the plus to show

Variation displays