Original source

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

Alleles
C/G|Ancestral: G|Ambiguity code: S|MAF: 0.27 (G)
Location

Chromosome 3:70952104 (forward strand)|View in location tab

Most severe consequence
 
Downstream gene variant
Evidence status

HGVS name

3:g.70952104C>G

About this variant

This variant overlaps 4 transcripts, has 2846 sample genotypes and is mentioned in 1 citation.

Variant displays