Original source

Variants (including SNPs and indels) imported from dbSNP (release 140) | [View in dbSNP]

G/A | Ambiguity code: R

Chromosome 6:36523367 (forward strand) | View in location tab

Most severe consequence
Evidence status


NextGen Project ss1174505924

This variation has 3 HGVS names - click the plus to show

About this variant

This variant overlaps 2 transcripts and has 160 individual genotypes.

Variation displays