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: 0.25 (T)
Location

Chromosome 2:191099907 (forward strand) | View in location tab

Most severe consequence
Evidence status

Clinical significance

Synonyms

Archive dbSNP rs57433953, rs52795984

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

2:g.191099907T>G
ENST00000358470.5:c.274-23582A>C
ENST00000392320.3:c.274-23582A>C
ENST00000495849.2:n.342-23582A>C
ENST00000495326.1:n.344-23582A>C
ENST00000413064.2:c.193-23582A>C

This variation has assays on 11 chips - click the plus to show

Variation displays