Original source

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

Alleles
C/T | Ancestral: T | Ambiguity code: Y | MAF: 0.27 (T)
Location

Chromosome 1:116908411 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

1:g.116908411C>T

About this variant

This variant overlaps 3 transcripts and has 2506 individual genotypes.

Variation displays