Original source

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

Alleles
T/- | Ancestral: T | MAF: 0.02 (-)
Location

Chromosome 2:236165254 (forward strand) | View in location tab

Co-located

with dbSNP rs4292047 (T/C)

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs67252683

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

Variation displays