Original source

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

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

Chromosome 2:111231795 (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.111231795T>G
ENST00000609220.1:n.39-34601A>C
ENST00000609902.3:n.328+1833A>C
ENST00000439362.3:n.636+1833A>C

This variation has assays on 8 chips - click the plus to show

Variation displays