Original source

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

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

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

Most severe consequence
Upstream gene variant
Evidence status

HGVS name


About this variant

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

Variant displays