Original source

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

Alleles
T/C | Ancestral: C | Ambiguity code: Y | MAF: 0.21 (T)
Location

Chromosome 9:133635393 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CR014914

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs60944937

HGVS name

9:g.133635393T>C

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

Variation displays