Original source

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

Alleles
T/C | Ancestral: T | Ambiguity code: Y | MAF: 0.02 (C)
Location

Chromosome 1:2227589 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

1:g.2227589T>C

About this variant

This variant overlaps 3 transcripts and has 2504 individual genotypes.

Variation displays