Original source

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

Alleles
C/T | Ancestral: G | Ambiguity code: Y | MAF: 0.20 (T)
Location

Chromosome 1:230281625 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs3811483

This variation has 4 HGVS names - click the plus to show

1:g.230281625C>T
ENST00000414640.1:n.269G>A
ENST00000366672.4:c.*2167C>T
ENST00000485438.1:n.3535C>T

This variation has assays on 6 chips - click the plus to show

Variation displays