Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.27 (T)
Location

Chromosome 10:50816943 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs60083637

HGVS name

10:g.50816943C>T

This variation has assays on 4 chips - click the plus to show

Variation displays