Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|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 variant

HGMD-PUBLIC CR972844

Most severe consequence
 
Upstream gene variant
Evidence status

Synonyms

Archive dbSNP rs61203218, rs36213154

HGVS name

13:g.46897343C>T

Genotyping chips

This variant has assays on 10 chips - Show

About this variant

This variant overlaps 4 transcripts, has 3764 sample genotypes and is mentioned in 84 citations.

Variant displays