Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
T/C | Ancestral: T | Ambiguity code: Y | MAF: 0.01 (C)
Location

Chromosome 4:73738938 (forward strand) | View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

HGVS name

4:g.73738938T>C

About this variant

This variant overlaps 3 transcripts, has 2504 sample genotypes and is mentioned in 1 citation.

Variant displays