Original source

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

Alleles
T/C | Ancestral: T | Ambiguity code: Y | MAF: 0.31 (C)
Location

Chromosome 4:155534408 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms
HGVS name

4:g.155534408T>C

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

Variation displays