Original source

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

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

Chromosome 11:102669824 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CR082027

Most severe consequence
Evidence status

This variation has 8 HGVS names - click the plus to show

HG305_PATCH:g.102669824A>G
ENST00000572001.1:n.443+971A>G
11:g.102669824A>G
ENST00000525739.2:n.682+971A>G
ENST00000572697.1:n.682+971A>G
ENST00000371455.3:n.423+971A>G
ENST00000575579.1:n.423+971A>G
ENST00000544704.1:n.443+971A>G

Genotyping chips

This variation has assays on: Illumina_1M-duo, Illumina_HumanOmni1-Quad, Illumina_HumanOmni2.5

Variation displays