Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

Alleles
C/G|Ancestral: G|Ambiguity code: S|MAF: 0.41 (C)
Location

Chromosome 10:98456807 (forward strand)|View in location tab

Most severe consequence
 
Downstream gene variant
Evidence status

HGVS name

10:g.98456807C>G

About this variant

This variant overlaps 5 transcripts and has 2510 sample genotypes.

Variant displays