Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | View in dbSNP

Alleles
A/G | Ancestral: A | Ambiguity code: R | MAF: 0.12 (G)
Location

Chromosome 11:102799093 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CR082027

Most severe consequence
Evidence status

This variation has 4 HGVS names - click the plus to show

11:g.102799093A>G
ENST00000525739.3:n.682+971A>G
ENST00000371455.4:n.423+971A>G
ENST00000544704.1:n.443+971A>G

This variation has assays on 4 chips - click the plus to show

Variation displays