Original source

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

Alleles
T/G | Ancestral: T | Ambiguity code: K | MAF: 0.25 (T)
Location

Chromosome 2:191964633 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs57433953, rs52795984

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

2:g.191964633T>G
ENST00000358470.4:c.274-23582A>C
ENST00000392320.2:c.274-23582A>C
ENST00000495849.1:n.342-23582A>C
ENST00000495326.1:n.344-23582A>C
ENST00000413064.1:c.193-23582A>C

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

Variation displays