Original source

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

Alleles
T/C|Ancestral: C|Ambiguity code: Y|MAF: 0.32 (T)
Location

Chromosome 4:53377063 (forward strand)|View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

Synonyms

Archive dbSNP rs56997400

HGVS name

4:g.53377063T>C

About this variant

This variant overlaps 9 transcripts and has 2781 sample genotypes.

Variant displays