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: 0.19 (T)
Location

Chromosome 17:47300211 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs57072022

This variation has 3 HGVS names - click the plus to show

17:g.47300211G>T
ENST00000559488.3:c.1914-267G>T
ENST00000560629.1:c.1879-267G>T

This variation has assays on 10 chips - click the plus to show

Variation displays