Original source

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

Alleles
A/T | Ancestral: A | Ambiguity code: W
Location

Chromosome 9:99103745 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

9:g.99103745A>T

About this variant

This variant overlaps 6 transcripts and has 89 individual genotypes.

Variation displays