Original source

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

Alleles
A/G | Ancestral: G | Ambiguity code: R | MAF: 0.44 (A)
Location

Chromosome 4:122277280 (forward strand) | View in location tab

Most severe consequence
Evidence status

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

4:g.122277280A>G
ENST00000264501.6:c.8591+1258A>G
ENST00000388738.5:c.8591+1258A>G
ENST00000419325.3:c.2463+1258A>G

Genotyping chips

This variation has assays on: Illumina_ExomeChip

Variation displays