Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.15 (C)
Location

Chromosome 6:137320867 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs1775299, rs58994219

HGVS name

6:g.137320867C>T

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

Variation displays