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 1:12165876 (forward strand) | View in location tab

Most severe consequence
Upstream gene variant
Evidence status

HGVS name


About this variant

This variant overlaps 4 transcripts, has 2582 sample genotypes and is mentioned in 1 citation.

Variant displays