Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.44 (T)
Location

Chromosome 13:46897343 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CR972844

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs61203218, rs36213154

HGVS name

13:g.46897343C>T

This variation has assays on 10 chips - click the plus to show

Variation displays