Original source

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

Alleles
C/A | Ancestral: C | Ambiguity code: M | MAF: 0.04 (A)
Location

Chromosome 10:98456802 (forward strand) | View in location tab

Most severe consequence
 
Downstream gene variant
Evidence status

HGVS name

10:g.98456802C>A

About this variant

This variant overlaps 5 transcripts and has 2505 sample genotypes.

Variant displays