Original source

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

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

Chromosome 17:65528964 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

This variation has 6 HGVS names - click the plus to show

17:g.65528964A>T
ENST00000618960.2:c.*1012T>A
ENST00000307078.7:c.*1012T>A
ENST00000611991.1:c.397-264T>A
LRG_296:g.37659T>A
LRG_296t1:c.*1012T>A

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

Variation displays