Original source

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

Alleles
G/T | Ancestral: G | Ambiguity code: K | MAF: 0.39 (G)
Location

Chromosome 17:82209113 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs57599031

This variation has 5 HGVS names - click the plus to show

17:g.82209113G>T
ENST00000389641.5:c.-9+3672C>A
ENST00000582885.1:n.52-1065C>A
ENST00000392343.3:c.-326-1065C>A
ENST00000392347.2:c.-9+3672C>A

This variation has assays on 5 chips - click the plus to show

Variation displays