Original source

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

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

Chromosome 9:99104009 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

9:g.99104009C>T

This variation has assays on 5 chips - click the plus to show

About this variant

This variant overlaps 7 transcripts and has 3194 individual genotypes.

Variation displays