Original source

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

Alleles
T/G | Ancestral: T | Ambiguity code: K | MAF: 0.08 (G)
Location

Chromosome 2:111989372 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs17808494

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

2:g.111989372T>G
ENST00000609220.1:n.39-34601A>C
ENST00000609902.1:n.328+1833A>C
ENST00000439362.1:n.636+1833A>C

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

Variation displays