Original source

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

Alleles
C/T | Ancestral: T | Ambiguity code: Y | MAF: 0.39 (T)
Location

Chromosome 2:234158839 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs57072142

This variation has 2 HGVS names - click the plus to show

2:g.234158839C>T
ENST00000431917.1:c.-137-5909C>T

This variation has assays on 7 chips - click the plus to show

Variation displays