Original source

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

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

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

Most severe consequence
Downstream gene variant
Evidence status

HGVS name


About this variant

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

Variant displays